Baxter Healthcare Corporation Discontinued
FDA Approved Drugs
Baxter Healthcare Corporation Discontinued
FDA Approved Drugs Database
FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.
- Total Records 212
- Latest Approval Date Sep 17, 2025
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Overview
Company
Baxter Healthcare Corporation Discontinued
Country
U.S.A
Website
Social Profiles
Company Snapshot
Baxter Healthcare Corporation Discontinued
One Baxter Parkway Deerfield, IL 60015-4625
U.S.A
www.baxter.com/ onebaxter@baxter.com View on MapFDA Approved Drug Records ( 212 records )
Drug Name
AMINOCAPROIC ACID
Product Number
1
Dosage Form
-
Strength
250MG/ML
Approval Date
1982-10-29
Active Ingredient
AMINOCAPROIC ACID
Application Number
18590
Product Number
1
Dosage Form
-
Strength
250MG/ML
Approval Date
1982-10-29
Regulatory Status
Discontinued
Drug Name
AMRINONE LACTATE
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
2000-05-10
Active Ingredient
INAMRINONE LACTATE
Application Number
75542
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
2000-05-10
Regulatory Status
Discontinued
Drug Name
ANCEF IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
EQ 10MG BASE/ML
Approval Date
1983-06-08
Active Ingredient
CEFAZOLIN SODIUM
Application Number
50566
Product Number
3
Dosage Form
-
Strength
EQ 10MG BASE/ML
Approval Date
1983-06-08
Regulatory Status
Discontinued
Drug Name
ANCEF IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1983-06-08
Active Ingredient
CEFAZOLIN SODIUM
Application Number
50566
Product Number
4
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1983-06-08
Regulatory Status
Discontinued
Drug Name
ANCEF IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE/ML
Approval Date
1991-03-28
Active Ingredient
CEFAZOLIN SODIUM
Application Number
63002
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE/ML
Approval Date
1991-03-28
Regulatory Status
Discontinued
Drug Name
ANCEF IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1991-03-28
Active Ingredient
CEFAZOLIN SODIUM
Application Number
63002
Product Number
2
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1991-03-28
Regulatory Status
Discontinued
Drug Name
ANCEF IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE/ML
Approval Date
1983-06-08
Active Ingredient
CEFAZOLIN SODIUM
Application Number
50566
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE/ML
Approval Date
1983-06-08
Regulatory Status
Discontinued
Drug Name
ANCEF IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1983-06-08
Active Ingredient
CEFAZOLIN SODIUM
Application Number
50566
Product Number
2
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1983-06-08
Regulatory Status
Discontinued
Drug Name
ATRACURIUM BESYLATE
Product Number
1
Dosage Form
-
Strength
10MG/ML
Approval Date
1997-01-23
Active Ingredient
ATRACURIUM BESYLATE
Application Number
74753
Product Number
1
Dosage Form
-
Strength
10MG/ML
Approval Date
1997-01-23
Regulatory Status
Discontinued
Drug Name
ATRACURIUM BESYLATE
Product Number
1
Dosage Form
-
Strength
10MG/ML
Approval Date
1997-09-30
Active Ingredient
ATRACURIUM BESYLATE
Application Number
74824
Product Number
1
Dosage Form
-
Strength
10MG/ML
Approval Date
1997-09-30
Regulatory Status
Discontinued
Drug Name
ATRACURIUM BESYLATE PRESERVATIVE FREE
Product Number
1
Dosage Form
-
Strength
10MG/ML
Approval Date
1997-01-23
Active Ingredient
ATRACURIUM BESYLATE
Application Number
74768
Product Number
1
Dosage Form
-
Strength
10MG/ML
Approval Date
1997-01-23
Regulatory Status
Discontinued
Drug Name
ATRACURIUM BESYLATE PRESERVATIVE FREE
Product Number
1
Dosage Form
-
Strength
10MG/ML
Approval Date
1997-09-30
Active Ingredient
ATRACURIUM BESYLATE
Application Number
74825
Product Number
1
Dosage Form
-
Strength
10MG/ML
Approval Date
1997-09-30
Regulatory Status
Discontinued
Drug Name
BACTOCILL IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1989-10-26
Active Ingredient
OXACILLIN SODIUM
Application Number
50640
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1989-10-26
Regulatory Status
Discontinued
Drug Name
BIVALIRUDIN IN 0.9% SODIUM CHLORIDE
Product Number
1
Dosage Form
-
Strength
250MG/50ML (5MG/ML)
Approval Date
2017-12-21
Active Ingredient
BIVALIRUDIN
Application Number
208374
Product Number
1
Dosage Form
-
Strength
250MG/50ML (5MG/ML)
Approval Date
2017-12-21
Regulatory Status
Discontinued
Drug Name
BIVALIRUDIN IN 0.9% SODIUM CHLORIDE
Product Number
2
Dosage Form
-
Strength
500MG/100ML (5MG/ML)
Approval Date
2017-12-21
Active Ingredient
BIVALIRUDIN
Application Number
208374
Product Number
2
Dosage Form
-
Strength
500MG/100ML (5MG/ML)
Approval Date
2017-12-21
Regulatory Status
Discontinued
Drug Name
BORTEZOMIB
Product Number
1
Dosage Form
-
Strength
3.5MG/VIAL
Approval Date
2022-05-02
Active Ingredient
BORTEZOMIB
Application Number
213823
Product Number
1
Dosage Form
-
Strength
3.5MG/VIAL
Approval Date
2022-05-02
Regulatory Status
Discontinued
Drug Name
BRANCHAMIN 4%
Product Number
1
Dosage Form
-
Strength
4% (4GM/100ML)
Approval Date
1984-09-28
Active Ingredient
AMINO ACIDS
Application Number
18678
Product Number
1
Dosage Form
-
Strength
4% (4GM/100ML)
Approval Date
1984-09-28
Regulatory Status
Discontinued
Drug Name
BRANCHAMIN 4% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
4% (4GM/100ML)
Approval Date
1984-09-28
Active Ingredient
AMINO ACIDS
Application Number
18684
Product Number
1
Dosage Form
-
Strength
4% (4GM/100ML)
Approval Date
1984-09-28
Regulatory Status
Discontinued
Drug Name
BRETYLIUM TOSYLATE IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
400MG/100ML
Approval Date
1989-04-12
Active Ingredient
BRETYLIUM TOSYLATE
Application Number
19837
Product Number
1
Dosage Form
-
Strength
400MG/100ML
Approval Date
1989-04-12
Regulatory Status
Discontinued
Drug Name
BRETYLIUM TOSYLATE IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
200MG/100ML
Approval Date
1989-04-12
Active Ingredient
BRETYLIUM TOSYLATE
Application Number
19837
Product Number
2
Dosage Form
-
Strength
200MG/100ML
Approval Date
1989-04-12
Regulatory Status
Discontinued
Drug Name
BREVIBLOC
Product Number
3
Dosage Form
-
Strength
10MG/ML
Approval Date
1988-08-15
Active Ingredient
ESMOLOL HYDROCHLORIDE
Application Number
19386
Product Number
3
Dosage Form
-
Strength
10MG/ML
Approval Date
1988-08-15
Regulatory Status
Discontinued
Drug Name
BREVIBLOC
Product Number
7
Dosage Form
-
Strength
20MG/ML
Approval Date
2003-05-28
Active Ingredient
ESMOLOL HYDROCHLORIDE
Application Number
19386
Product Number
7
Dosage Form
-
Strength
20MG/ML
Approval Date
2003-05-28
Regulatory Status
Discontinued
Drug Name
BUPIVACAINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
0.75%
Approval Date
2016-07-25
Active Ingredient
BUPIVACAINE HYDROCHLORIDE
Application Number
207266
Product Number
1
Dosage Form
-
Strength
0.75%
Approval Date
2016-07-25
Regulatory Status
Discontinued
Drug Name
BUTORPHANOL TARTRATE
Product Number
1
Dosage Form
-
Strength
2MG/ML
Approval Date
2001-10-23
Active Ingredient
BUTORPHANOL TARTRATE
Application Number
75697
Product Number
1
Dosage Form
-
Strength
2MG/ML
Approval Date
2001-10-23
Regulatory Status
Discontinued
Drug Name
BUTORPHANOL TARTRATE PRESERVATIVE FREE
Product Number
1
Dosage Form
-
Strength
1MG/ML
Approval Date
2001-10-23
Active Ingredient
BUTORPHANOL TARTRATE
Application Number
75695
Product Number
1
Dosage Form
-
Strength
1MG/ML
Approval Date
2001-10-23
Regulatory Status
Discontinued
Drug Name
BUTORPHANOL TARTRATE PRESERVATIVE FREE
Product Number
2
Dosage Form
-
Strength
2MG/ML
Approval Date
2001-10-23
Active Ingredient
BUTORPHANOL TARTRATE
Application Number
75695
Product Number
2
Dosage Form
-
Strength
2MG/ML
Approval Date
2001-10-23
Regulatory Status
Discontinued
Drug Name
CEFTAZIDIME SODIUM IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE/ML
Approval Date
1993-04-29
Active Ingredient
CEFTAZIDIME SODIUM
Application Number
63221
Product Number
1
Dosage Form
-
Strength
EQ 10MG BASE/ML
Approval Date
1993-04-29
Regulatory Status
Discontinued
Drug Name
CEFTAZIDIME SODIUM IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1993-04-29
Active Ingredient
CEFTAZIDIME SODIUM
Application Number
63221
Product Number
2
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1993-04-29
Regulatory Status
Discontinued
Drug Name
CEFTAZIDIME SODIUM IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
EQ 40MG BASE/ML
Approval Date
1993-04-29
Active Ingredient
CEFTAZIDIME SODIUM
Application Number
63221
Product Number
3
Dosage Form
-
Strength
EQ 40MG BASE/ML
Approval Date
1993-04-29
Regulatory Status
Discontinued
Drug Name
CEPHALOTHIN SODIUM W/ DEXTROSE IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1984-01-31
Active Ingredient
CEPHALOTHIN SODIUM
Application Number
62422
Product Number
3
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1984-01-31
Regulatory Status
Discontinued
Drug Name
CEPHALOTHIN SODIUM W/ DEXTROSE IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
EQ 40MG BASE/ML
Approval Date
1984-01-31
Active Ingredient
CEPHALOTHIN SODIUM
Application Number
62422
Product Number
4
Dosage Form
-
Strength
EQ 40MG BASE/ML
Approval Date
1984-01-31
Regulatory Status
Discontinued
Drug Name
CEPHALOTHIN SODIUM W/ DEXTROSE IN PLASTIC CONTAINER
Product Number
5
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1991-07-16
Active Ingredient
CEPHALOTHIN SODIUM
Application Number
62422
Product Number
5
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1991-07-16
Regulatory Status
Discontinued
Drug Name
CEPHALOTHIN SODIUM W/ DEXTROSE IN PLASTIC CONTAINER
Product Number
6
Dosage Form
-
Strength
EQ 40MG BASE/ML
Approval Date
1991-07-16
Active Ingredient
CEPHALOTHIN SODIUM
Application Number
62422
Product Number
6
Dosage Form
-
Strength
EQ 40MG BASE/ML
Approval Date
1991-07-16
Regulatory Status
Discontinued
Drug Name
CEPHALOTHIN SODIUM W/ DEXTROSE IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1987-03-05
Active Ingredient
CEPHALOTHIN SODIUM
Application Number
62730
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1987-03-05
Regulatory Status
Discontinued
Drug Name
CEPHALOTHIN SODIUM W/ DEXTROSE IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
EQ 40MG BASE/ML
Approval Date
1987-03-05
Active Ingredient
CEPHALOTHIN SODIUM
Application Number
62730
Product Number
2
Dosage Form
-
Strength
EQ 40MG BASE/ML
Approval Date
1987-03-05
Regulatory Status
Discontinued
Drug Name
CEPHALOTHIN SODIUM W/ SODIUM CHLORIDE IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1984-01-31
Active Ingredient
CEPHALOTHIN SODIUM
Application Number
62422
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1984-01-31
Regulatory Status
Discontinued
Drug Name
CEPHALOTHIN SODIUM W/ SODIUM CHLORIDE IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
EQ 40MG BASE/ML
Approval Date
1984-01-31
Active Ingredient
CEPHALOTHIN SODIUM
Application Number
62422
Product Number
2
Dosage Form
-
Strength
EQ 40MG BASE/ML
Approval Date
1984-01-31
Regulatory Status
Discontinued
Drug Name
CIPROFLOXACIN
Product Number
1
Dosage Form
-
Strength
200MG/20ML (10MG/ML)
Approval Date
2008-04-29
Active Ingredient
CIPROFLOXACIN
Application Number
78062
Product Number
1
Dosage Form
-
Strength
200MG/20ML (10MG/ML)
Approval Date
2008-04-29
Regulatory Status
Discontinued
Drug Name
CIPROFLOXACIN
Product Number
2
Dosage Form
-
Strength
400MG/40ML (10MG/ML)
Approval Date
2008-04-29
Active Ingredient
CIPROFLOXACIN
Application Number
78062
Product Number
2
Dosage Form
-
Strength
400MG/40ML (10MG/ML)
Approval Date
2008-04-29
Regulatory Status
Discontinued
Drug Name
CIPROFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
200MG/100ML
Approval Date
2008-03-18
Active Ingredient
CIPROFLOXACIN
Application Number
77888
Product Number
1
Dosage Form
-
Strength
200MG/100ML
Approval Date
2008-03-18
Regulatory Status
Discontinued
Drug Name
CIPROFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
400MG/200ML
Approval Date
2008-03-18
Active Ingredient
CIPROFLOXACIN
Application Number
77888
Product Number
2
Dosage Form
-
Strength
400MG/200ML
Approval Date
2008-03-18
Regulatory Status
Discontinued
Drug Name
CIPROFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
200MG/100ML
Approval Date
2008-03-18
Active Ingredient
CIPROFLOXACIN
Application Number
78024
Product Number
1
Dosage Form
-
Strength
200MG/100ML
Approval Date
2008-03-18
Regulatory Status
Discontinued
Drug Name
CIPROFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
400MG/200ML
Approval Date
2008-03-18
Active Ingredient
CIPROFLOXACIN
Application Number
78024
Product Number
2
Dosage Form
-
Strength
400MG/200ML
Approval Date
2008-03-18
Regulatory Status
Discontinued
Drug Name
CLINDAMYCIN PHOSPHATE IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
EQ 6MG BASE/ML
Approval Date
1989-12-29
Active Ingredient
CLINDAMYCIN PHOSPHATE
Application Number
50648
Product Number
1
Dosage Form
-
Strength
EQ 6MG BASE/ML
Approval Date
1989-12-29
Regulatory Status
Discontinued
Drug Name
CLINDAMYCIN PHOSPHATE IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
EQ 12MG BASE/ML
Approval Date
1989-12-29
Active Ingredient
CLINDAMYCIN PHOSPHATE
Application Number
50648
Product Number
2
Dosage Form
-
Strength
EQ 12MG BASE/ML
Approval Date
1989-12-29
Regulatory Status
Discontinued
Drug Name
CLINDAMYCIN PHOSPHATE IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
EQ 900MG BASE/100ML
Approval Date
1989-12-29
Active Ingredient
CLINDAMYCIN PHOSPHATE
Application Number
50648
Product Number
3
Dosage Form
-
Strength
EQ 900MG BASE/100ML
Approval Date
1989-12-29
Regulatory Status
Discontinued
Drug Name
CYCLOPHOSPHAMIDE
Product Number
1
Dosage Form
-
Strength
100MG/VIAL
Approval Date
1986-07-03
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
88371
Product Number
1
Dosage Form
-
Strength
100MG/VIAL
Approval Date
1986-07-03
Regulatory Status
Discontinued
Drug Name
CYCLOPHOSPHAMIDE
Product Number
1
Dosage Form
-
Strength
200MG/VIAL
Approval Date
1986-07-03
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
88372
Product Number
1
Dosage Form
-
Strength
200MG/VIAL
Approval Date
1986-07-03
Regulatory Status
Discontinued
Drug Name
CYCLOPHOSPHAMIDE
Product Number
1
Dosage Form
-
Strength
500MG/VIAL
Approval Date
1986-07-03
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
88373
Product Number
1
Dosage Form
-
Strength
500MG/VIAL
Approval Date
1986-07-03
Regulatory Status
Discontinued
Drug Name
CYCLOPHOSPHAMIDE
Product Number
1
Dosage Form
-
Strength
1GM/VIAL
Approval Date
1986-09-24
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
88374
Product Number
1
Dosage Form
-
Strength
1GM/VIAL
Approval Date
1986-09-24
Regulatory Status
Discontinued
Drug Name
CYTOXAN
Product Number
1
Dosage Form
-
Strength
100MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
12142
Product Number
1
Dosage Form
-
Strength
100MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CYTOXAN
Product Number
2
Dosage Form
-
Strength
200MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
12142
Product Number
2
Dosage Form
-
Strength
200MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CYTOXAN (LYOPHILIZED)
Product Number
3
Dosage Form
-
Strength
500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
12142
Product Number
3
Dosage Form
-
Strength
500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CYTOXAN (LYOPHILIZED)
Product Number
4
Dosage Form
-
Strength
1GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-08-30
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
12142
Product Number
4
Dosage Form
-
Strength
1GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-08-30
Regulatory Status
Discontinued
Drug Name
CYTOXAN (LYOPHILIZED)
Product Number
5
Dosage Form
-
Strength
2GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-08-30
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
12142
Product Number
5
Dosage Form
-
Strength
2GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-08-30
Regulatory Status
Discontinued
Drug Name
CYTOXAN (LYOPHILIZED)
Product Number
8
Dosage Form
-
Strength
500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-01-04
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
12142
Product Number
8
Dosage Form
-
Strength
500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-01-04
Regulatory Status
Discontinued
Drug Name
CYTOXAN (LYOPHILIZED)
Product Number
9
Dosage Form
-
Strength
2GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-12-10
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
12142
Product Number
9
Dosage Form
-
Strength
2GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-12-10
Regulatory Status
Discontinued
Drug Name
CYTOXAN (LYOPHILIZED)
Product Number
10
Dosage Form
-
Strength
1GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-09-24
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
12142
Product Number
10
Dosage Form
-
Strength
1GM/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-09-24
Regulatory Status
Discontinued
Drug Name
DAPZURA RT
Product Number
1
Dosage Form
-
Strength
500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2022-01-25
Active Ingredient
DAPTOMYCIN
Application Number
213645
Product Number
1
Dosage Form
-
Strength
500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2022-01-25
Regulatory Status
Discontinued
Drug Name
DEXTROSE 10% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
10GM/100ML;900MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; SODIUM CHLORIDE
Application Number
16696
Product Number
1
Dosage Form
-
Strength
10GM/100ML;900MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 20% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
20GM/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
DEXTROSE
Application Number
17521
Product Number
4
Dosage Form
-
Strength
20GM/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 30% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
30GM/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
DEXTROSE
Application Number
17521
Product Number
3
Dosage Form
-
Strength
30GM/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 40% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
40GM/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
DEXTROSE
Application Number
17521
Product Number
2
Dosage Form
-
Strength
40GM/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5% AND ELECTROLYTE NO. 75 IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5GM/100ML;205MG/100ML;100MG/100ML;120MG/100ML;220MG/100ML
Approval Date
1983-06-29
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM CHLORIDE; SODIUM LACTATE
Application Number
18840
Product Number
1
Dosage Form
-
Strength
5GM/100ML;205MG/100ML;100MG/100ML;120MG/100ML;220MG/100ML
Approval Date
1983-06-29
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5% IN RINGERS IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
33MG/100ML;5GM/100ML;30MG/100ML;860MG/100ML
Approval Date
1982-01-01
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
16695
Product Number
1
Dosage Form
-
Strength
33MG/100ML;5GM/100ML;30MG/100ML;860MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5%, SODIUM CHLORIDE 0.45% AND POTASSIUM CHLORIDE 15MEQ IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
5GM/100ML;224MG/100ML;450MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18008
Product Number
3
Dosage Form
-
Strength
5GM/100ML;224MG/100ML;450MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5%, SODIUM CHLORIDE 0.45% AND POTASSIUM CHLORIDE 20MEQ (K) IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5GM/100ML;300MG/100ML;450MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18008
Product Number
1
Dosage Form
-
Strength
5GM/100ML;300MG/100ML;450MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5%, SODIUM CHLORIDE 0.45% AND POTASSIUM CHLORIDE 5MEQ IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
5GM/100ML;75MG/100ML;450MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18008
Product Number
2
Dosage Form
-
Strength
5GM/100ML;75MG/100ML;450MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 50% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
50GM/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
DEXTROSE
Application Number
17521
Product Number
1
Dosage Form
-
Strength
50GM/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 60% IN PLASTIC CONTAINER
Product Number
5
Dosage Form
-
Strength
60GM/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-03-26
Active Ingredient
DEXTROSE
Application Number
17521
Product Number
5
Dosage Form
-
Strength
60GM/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-03-26
Regulatory Status
Discontinued
Drug Name
DEXTROSE 60% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
60GM/100ML
Approval Date
1991-07-02
Active Ingredient
DEXTROSE
Application Number
20047
Product Number
2
Dosage Form
-
Strength
60GM/100ML
Approval Date
1991-07-02
Regulatory Status
Discontinued
Drug Name
DEXTROSE 70% IN PLASTIC CONTAINER
Product Number
6
Dosage Form
-
Strength
70GM/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-03-26
Active Ingredient
DEXTROSE
Application Number
17521
Product Number
6
Dosage Form
-
Strength
70GM/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-03-26
Regulatory Status
Discontinued
Drug Name
DIHYDROERGOTAMINE MESYLATE
Product Number
1
Dosage Form
-
Strength
1MG/ML
Approval Date
2025-01-07
Active Ingredient
DIHYDROERGOTAMINE MESYLATE
Application Number
216747
Product Number
1
Dosage Form
-
Strength
1MG/ML
Approval Date
2025-01-07
Regulatory Status
Discontinued
Drug Name
DIMENHYDRINATE
Product Number
1
Dosage Form
-
Strength
50MG/ML
Approval Date
1982-01-01
Active Ingredient
DIMENHYDRINATE
Application Number
84767
Product Number
1
Dosage Form
-
Strength
50MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DOBUTAMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 12.5MG BASE/ML
Approval Date
1996-09-26
Active Ingredient
DOBUTAMINE HYDROCHLORIDE
Application Number
74381
Product Number
1
Dosage Form
-
Strength
EQ 12.5MG BASE/ML
Approval Date
1996-09-26
Regulatory Status
Discontinued
Drug Name
DOPAMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
40MG/ML
Approval Date
1982-01-01
Active Ingredient
DOPAMINE HYDROCHLORIDE
Application Number
18398
Product Number
1
Dosage Form
-
Strength
40MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DOPAMINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
80MG/ML
Approval Date
1982-03-22
Active Ingredient
DOPAMINE HYDROCHLORIDE
Application Number
18398
Product Number
2
Dosage Form
-
Strength
80MG/ML
Approval Date
1982-03-22
Regulatory Status
Discontinued
Drug Name
EPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 16MG BASE/250ML (EQ 64MCG BASE/ML)
Approval Date
2025-02-28
Active Ingredient
EPINEPHRINE BITARTRATE
Application Number
218475
Product Number
1
Dosage Form
-
Strength
EQ 16MG BASE/250ML (EQ 64MCG BASE/ML)
Approval Date
2025-02-28
Regulatory Status
Discontinued
Drug Name
EPTIFIBATIDE
Product Number
1
Dosage Form
-
Strength
2MG/ML
Approval Date
2018-11-23
Active Ingredient
EPTIFIBATIDE
Application Number
208554
Product Number
1
Dosage Form
-
Strength
2MG/ML
Approval Date
2018-11-23
Regulatory Status
Discontinued
Drug Name
ERYTHROMYCIN LACTOBIONATE
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
1989-05-09
Active Ingredient
ERYTHROMYCIN LACTOBIONATE
Application Number
62993
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
1989-05-09
Regulatory Status
Discontinued
Drug Name
ERYTHROMYCIN LACTOBIONATE
Product Number
2
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
1989-05-09
Active Ingredient
ERYTHROMYCIN LACTOBIONATE
Application Number
62993
Product Number
2
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
1989-05-09
Regulatory Status
Discontinued
Drug Name
ETHRANE
Product Number
1
Dosage Form
-
Strength
99.9% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
ENFLURANE
Application Number
17087
Product Number
1
Dosage Form
-
Strength
99.9% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
FLUCONAZOLE IN SODIUM CHLORIDE 0.9%
Product Number
1
Dosage Form
-
Strength
200MG/100ML (2MG/ML)
Approval Date
2010-05-26
Active Ingredient
FLUCONAZOLE
Application Number
77947
Product Number
1
Dosage Form
-
Strength
200MG/100ML (2MG/ML)
Approval Date
2010-05-26
Regulatory Status
Discontinued
Drug Name
FLUCONAZOLE IN SODIUM CHLORIDE 0.9%
Product Number
2
Dosage Form
-
Strength
400MG/200ML (2MG/ML)
Approval Date
2010-05-26
Active Ingredient
FLUCONAZOLE
Application Number
77947
Product Number
2
Dosage Form
-
Strength
400MG/200ML (2MG/ML)
Approval Date
2010-05-26
Regulatory Status
Discontinued
Drug Name
FOSAPREPITANT DIMEGLUMINE
Product Number
1
Dosage Form
-
Strength
EQ 150MG BASE/VIAL
Approval Date
2019-09-05
Active Ingredient
FOSAPREPITANT DIMEGLUMINE
Application Number
211860
Product Number
1
Dosage Form
-
Strength
EQ 150MG BASE/VIAL
Approval Date
2019-09-05
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
EQ 0.8MG BASE/ML
Approval Date
1982-09-07
Active Ingredient
GENTAMICIN SULFATE
Application Number
62373
Product Number
1
Dosage Form
-
Strength
EQ 0.8MG BASE/ML
Approval Date
1982-09-07
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
EQ 40MG BASE/100ML
Approval Date
1982-09-07
Active Ingredient
GENTAMICIN SULFATE
Application Number
62373
Product Number
3
Dosage Form
-
Strength
EQ 40MG BASE/100ML
Approval Date
1982-09-07
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
EQ 60MG BASE/100ML
Approval Date
1982-09-07
Active Ingredient
GENTAMICIN SULFATE
Application Number
62373
Product Number
4
Dosage Form
-
Strength
EQ 60MG BASE/100ML
Approval Date
1982-09-07
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
10
Dosage Form
-
Strength
EQ 2.4MG BASE/ML
Approval Date
1982-09-07
Active Ingredient
GENTAMICIN SULFATE
Application Number
62373
Product Number
10
Dosage Form
-
Strength
EQ 2.4MG BASE/ML
Approval Date
1982-09-07
Regulatory Status
Discontinued
Drug Name
GLYCINE 1.5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
1.5GM/100ML
Approval Date
1982-02-19
Active Ingredient
GLYCINE
Application Number
18522
Product Number
1
Dosage Form
-
Strength
1.5GM/100ML
Approval Date
1982-02-19
Regulatory Status
Discontinued
Drug Name
GRANISETRON HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)
Approval Date
2007-12-31
Active Ingredient
GRANISETRON HYDROCHLORIDE
Application Number
78197
Product Number
1
Dosage Form
-
Strength
EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)
Approval Date
2007-12-31
Regulatory Status
Discontinued
Drug Name
GRANISETRON HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 1MG BASE/ML (EQ 1MG BASE/ML)
Approval Date
2008-06-30
Active Ingredient
GRANISETRON HYDROCHLORIDE
Application Number
78198
Product Number
1
Dosage Form
-
Strength
EQ 1MG BASE/ML (EQ 1MG BASE/ML)
Approval Date
2008-06-30
Regulatory Status
Discontinued
Drug Name
GRANISETRON HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 4MG BASE/4ML (EQ 1MG BASE/ML)
Approval Date
2008-06-30
Active Ingredient
GRANISETRON HYDROCHLORIDE
Application Number
78198
Product Number
2
Dosage Form
-
Strength
EQ 4MG BASE/4ML (EQ 1MG BASE/ML)
Approval Date
2008-06-30
Regulatory Status
Discontinued
Drug Name
HALOPERIDOL
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
2004-08-25
Active Ingredient
HALOPERIDOL LACTATE
Application Number
76791
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
2004-08-25
Regulatory Status
Discontinued
Drug Name
HALOPERIDOL
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
2004-08-25
Active Ingredient
HALOPERIDOL LACTATE
Application Number
76828
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
2004-08-25
Regulatory Status
Discontinued
Drug Name
HEPARIN SODIUM 10,000 UNITS AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
2,000 UNITS/100ML
Approval Date
1985-07-09
Active Ingredient
HEPARIN SODIUM
Application Number
18814
Product Number
2
Dosage Form
-
Strength
2,000 UNITS/100ML
Approval Date
1985-07-09
Regulatory Status
Discontinued
Drug Name
HEPARIN SODIUM 20,000 UNITS AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
4,000 UNITS/100ML
Approval Date
1983-10-31
Active Ingredient
HEPARIN SODIUM
Application Number
18814
Product Number
1
Dosage Form
-
Strength
4,000 UNITS/100ML
Approval Date
1983-10-31
Regulatory Status
Discontinued
Drug Name
HEPARIN SODIUM 25,000 UNITS AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
5,000 UNITS/100ML
Approval Date
1985-07-09
Active Ingredient
HEPARIN SODIUM
Application Number
18814
Product Number
3
Dosage Form
-
Strength
5,000 UNITS/100ML
Approval Date
1985-07-09
Regulatory Status
Discontinued
Drug Name
HEPARIN SODIUM 25,000 UNITS AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
10,000 UNITS/100ML
Approval Date
1987-07-02
Active Ingredient
HEPARIN SODIUM
Application Number
18814
Product Number
4
Dosage Form
-
Strength
10,000 UNITS/100ML
Approval Date
1987-07-02
Regulatory Status
Discontinued
Drug Name
HEPARIN SODIUM 5,000 UNITS AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
500 UNITS/100ML
Approval Date
1982-04-28
Active Ingredient
HEPARIN SODIUM
Application Number
18609
Product Number
3
Dosage Form
-
Strength
500 UNITS/100ML
Approval Date
1982-04-28
Regulatory Status
Discontinued
Drug Name
HEPATASOL 8%
Product Number
1
Dosage Form
-
Strength
8% (8GM/100ML)
Approval Date
1996-04-04
Active Ingredient
AMINO ACIDS
Application Number
20360
Product Number
1
Dosage Form
-
Strength
8% (8GM/100ML)
Approval Date
1996-04-04
Regulatory Status
Discontinued
Drug Name
HYDROCORTISONE SODIUM SUCCINATE
Product Number
1
Dosage Form
-
Strength
EQ 100MG BASE/VIAL
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE SODIUM SUCCINATE
Application Number
86619
Product Number
1
Dosage Form
-
Strength
EQ 100MG BASE/VIAL
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDROCORTISONE SODIUM SUCCINATE
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/VIAL
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE SODIUM SUCCINATE
Application Number
87567
Product Number
1
Dosage Form
-
Strength
EQ 250MG BASE/VIAL
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDROCORTISONE SODIUM SUCCINATE
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE SODIUM SUCCINATE
Application Number
87568
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDROCORTISONE SODIUM SUCCINATE
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
1982-01-01
Active Ingredient
HYDROCORTISONE SODIUM SUCCINATE
Application Number
87569
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDROXYZINE
Product Number
2
Dosage Form
-
Strength
50MG/ML
Approval Date
1982-01-01
Active Ingredient
HYDROXYZINE HYDROCHLORIDE
Application Number
85551
Product Number
2
Dosage Form
-
Strength
50MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDROXYZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG/ML
Approval Date
1982-01-01
Active Ingredient
HYDROXYZINE HYDROCHLORIDE
Application Number
85551
Product Number
1
Dosage Form
-
Strength
25MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
IFEX/MESNEX KIT
Product Number
3
Dosage Form
-
Strength
1GM/VIAL;100MG/ML
Approval Date
1992-10-10
Active Ingredient
IFOSFAMIDE; MESNA
Application Number
19763
Product Number
3
Dosage Form
-
Strength
1GM/VIAL;100MG/ML
Approval Date
1992-10-10
Regulatory Status
Discontinued
Drug Name
IFEX/MESNEX KIT
Product Number
4
Dosage Form
-
Strength
3GM/VIAL;100MG/ML
Approval Date
1992-10-10
Active Ingredient
IFOSFAMIDE; MESNA
Application Number
19763
Product Number
4
Dosage Form
-
Strength
3GM/VIAL;100MG/ML
Approval Date
1992-10-10
Regulatory Status
Discontinued
Drug Name
IOPAMIDOL
Product Number
1
Dosage Form
-
Strength
41%
Approval Date
1996-11-06
Active Ingredient
IOPAMIDOL
Application Number
74629
Product Number
1
Dosage Form
-
Strength
41%
Approval Date
1996-11-06
Regulatory Status
Discontinued
Drug Name
IOPAMIDOL
Product Number
2
Dosage Form
-
Strength
61%
Approval Date
1996-11-06
Active Ingredient
IOPAMIDOL
Application Number
74629
Product Number
2
Dosage Form
-
Strength
61%
Approval Date
1996-11-06
Regulatory Status
Discontinued
Drug Name
IOPAMIDOL
Product Number
3
Dosage Form
-
Strength
76%
Approval Date
1996-11-06
Active Ingredient
IOPAMIDOL
Application Number
74629
Product Number
3
Dosage Form
-
Strength
76%
Approval Date
1996-11-06
Regulatory Status
Discontinued
Drug Name
IOPAMIDOL
Product Number
4
Dosage Form
-
Strength
51%
Approval Date
1998-03-31
Active Ingredient
IOPAMIDOL
Application Number
74629
Product Number
4
Dosage Form
-
Strength
51%
Approval Date
1998-03-31
Regulatory Status
Discontinued
Drug Name
IRRIGATING SOLUTION G IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
3.24GM/100ML;380MG/100ML;430MG/100ML
Approval Date
1982-06-22
Active Ingredient
CITRIC ACID; MAGNESIUM OXIDE; SODIUM CARBONATE
Application Number
18519
Product Number
1
Dosage Form
-
Strength
3.24GM/100ML;380MG/100ML;430MG/100ML
Approval Date
1982-06-22
Regulatory Status
Discontinued
Drug Name
ISOETHARINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
0.08%
Approval Date
1983-07-29
Active Ingredient
ISOETHARINE HYDROCHLORIDE
Application Number
88144
Product Number
1
Dosage Form
-
Strength
0.08%
Approval Date
1983-07-29
Regulatory Status
Discontinued
Drug Name
ISOETHARINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
0.14%
Approval Date
1984-03-26
Active Ingredient
ISOETHARINE HYDROCHLORIDE
Application Number
88145
Product Number
1
Dosage Form
-
Strength
0.14%
Approval Date
1984-03-26
Regulatory Status
Discontinued
Drug Name
ISOETHARINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
0.25%
Approval Date
1983-08-01
Active Ingredient
ISOETHARINE HYDROCHLORIDE
Application Number
88146
Product Number
1
Dosage Form
-
Strength
0.25%
Approval Date
1983-08-01
Regulatory Status
Discontinued
Drug Name
ISOPROTERENOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
0.2MG/ML
Approval Date
1982-01-01
Active Ingredient
ISOPROTERENOL HYDROCHLORIDE
Application Number
83486
Product Number
1
Dosage Form
-
Strength
0.2MG/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
KETAMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 100MG BASE/10ML (EQ 10MG BASE/ML)
Approval Date
2025-09-17
Active Ingredient
KETAMINE HYDROCHLORIDE
Application Number
219684
Product Number
1
Dosage Form
-
Strength
EQ 100MG BASE/10ML (EQ 10MG BASE/ML)
Approval Date
2025-09-17
Regulatory Status
Discontinued
Drug Name
KETOROLAC TROMETHAMINE
Product Number
1
Dosage Form
-
Strength
30MG/ML
Approval Date
2001-06-29
Active Ingredient
KETOROLAC TROMETHAMINE
Application Number
75631
Product Number
1
Dosage Form
-
Strength
30MG/ML
Approval Date
2001-06-29
Regulatory Status
Discontinued
Drug Name
KETOROLAC TROMETHAMINE
Product Number
2
Dosage Form
-
Strength
15MG/ML
Approval Date
2001-06-29
Active Ingredient
KETOROLAC TROMETHAMINE
Application Number
75631
Product Number
2
Dosage Form
-
Strength
15MG/ML
Approval Date
2001-06-29
Regulatory Status
Discontinued
Drug Name
LACTATED RINGERS IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
20MG/100ML;30MG/100ML;600MG/100ML;310MG/100ML
Approval Date
1989-08-29
Active Ingredient
CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Application Number
19933
Product Number
1
Dosage Form
-
Strength
20MG/100ML;30MG/100ML;600MG/100ML;310MG/100ML
Approval Date
1989-08-29
Regulatory Status
Discontinued
Drug Name
LEVOFLOXACIN
Product Number
1
Dosage Form
-
Strength
EQ 500MG/20ML (EQ 25MG/ML)
Approval Date
2013-06-05
Active Ingredient
LEVOFLOXACIN
Application Number
91436
Product Number
1
Dosage Form
-
Strength
EQ 500MG/20ML (EQ 25MG/ML)
Approval Date
2013-06-05
Regulatory Status
Discontinued
Drug Name
LEVOFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
EQ 250MG/50ML (EQ 5MG/ML)
Approval Date
2013-08-08
Active Ingredient
LEVOFLOXACIN
Application Number
91397
Product Number
1
Dosage Form
-
Strength
EQ 250MG/50ML (EQ 5MG/ML)
Approval Date
2013-08-08
Regulatory Status
Discontinued
Drug Name
LEVOFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
EQ 500MG/100ML (EQ 5MG/ML)
Approval Date
2013-08-08
Active Ingredient
LEVOFLOXACIN
Application Number
91397
Product Number
2
Dosage Form
-
Strength
EQ 500MG/100ML (EQ 5MG/ML)
Approval Date
2013-08-08
Regulatory Status
Discontinued
Drug Name
LEVOFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
EQ 750MG/150ML (EQ 5MG/ML)
Approval Date
2013-08-08
Active Ingredient
LEVOFLOXACIN
Application Number
91397
Product Number
3
Dosage Form
-
Strength
EQ 750MG/150ML (EQ 5MG/ML)
Approval Date
2013-08-08
Regulatory Status
Discontinued
Drug Name
LIDOCAINE HYDROCHLORIDE 0.1% AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
100MG/100ML
Approval Date
1982-01-01
Active Ingredient
LIDOCAINE HYDROCHLORIDE
Application Number
18461
Product Number
1
Dosage Form
-
Strength
100MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
LYOPHILIZED CYTOXAN
Product Number
6
Dosage Form
-
Strength
100MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-12-05
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
12142
Product Number
6
Dosage Form
-
Strength
100MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-12-05
Regulatory Status
Discontinued
Drug Name
LYOPHILIZED CYTOXAN
Product Number
7
Dosage Form
-
Strength
200MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-12-10
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
12142
Product Number
7
Dosage Form
-
Strength
200MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-12-10
Regulatory Status
Discontinued
Drug Name
MEPERIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG/ML
Approval Date
1984-06-15
Active Ingredient
MEPERIDINE HYDROCHLORIDE
Application Number
88279
Product Number
1
Dosage Form
-
Strength
25MG/ML
Approval Date
1984-06-15
Regulatory Status
Discontinued
Drug Name
MEPERIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
50MG/ML
Approval Date
1984-06-15
Active Ingredient
MEPERIDINE HYDROCHLORIDE
Application Number
88280
Product Number
1
Dosage Form
-
Strength
50MG/ML
Approval Date
1984-06-15
Regulatory Status
Discontinued
Drug Name
MEPERIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
75MG/ML
Approval Date
1984-06-15
Active Ingredient
MEPERIDINE HYDROCHLORIDE
Application Number
88281
Product Number
1
Dosage Form
-
Strength
75MG/ML
Approval Date
1984-06-15
Regulatory Status
Discontinued
Drug Name
MEPERIDINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
1984-06-15
Active Ingredient
MEPERIDINE HYDROCHLORIDE
Application Number
88282
Product Number
1
Dosage Form
-
Strength
100MG/ML
Approval Date
1984-06-15
Regulatory Status
Discontinued
Drug Name
METHOCARBAMOL
Product Number
1
Dosage Form
-
Strength
1GM/10ML (100MG/ML)
Approval Date
2022-07-14
Active Ingredient
METHOCARBAMOL
Application Number
215065
Product Number
1
Dosage Form
-
Strength
1GM/10ML (100MG/ML)
Approval Date
2022-07-14
Regulatory Status
Discontinued
Drug Name
METHYLDOPATE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
50MG/ML
Approval Date
1986-07-01
Active Ingredient
METHYLDOPATE HYDROCHLORIDE
Application Number
70291
Product Number
1
Dosage Form
-
Strength
50MG/ML
Approval Date
1986-07-01
Regulatory Status
Discontinued
Drug Name
METRONIDAZOLE IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
500MG/100ML
Approval Date
2008-03-31
Active Ingredient
METRONIDAZOLE
Application Number
78084
Product Number
1
Dosage Form
-
Strength
500MG/100ML
Approval Date
2008-03-31
Regulatory Status
Discontinued
Drug Name
MIDAZOLAM HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 1MG BASE/ML
Approval Date
2000-10-31
Active Ingredient
MIDAZOLAM HYDROCHLORIDE
Application Number
75637
Product Number
1
Dosage Form
-
Strength
EQ 1MG BASE/ML
Approval Date
2000-10-31
Regulatory Status
Discontinued
Drug Name
MIDAZOLAM HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
2000-10-31
Active Ingredient
MIDAZOLAM HYDROCHLORIDE
Application Number
75637
Product Number
2
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
2000-10-31
Regulatory Status
Discontinued
Drug Name
MILRINONE LACTATE
Product Number
1
Dosage Form
-
Strength
EQ 1MG BASE/ML
Approval Date
2004-09-21
Active Ingredient
MILRINONE LACTATE
Application Number
76427
Product Number
1
Dosage Form
-
Strength
EQ 1MG BASE/ML
Approval Date
2004-09-21
Regulatory Status
Discontinued
Drug Name
MILRINONE LACTATE IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/100ML (EQ 0.2MG BASE/ML)
Approval Date
2002-08-08
Active Ingredient
MILRINONE LACTATE
Application Number
76259
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/100ML (EQ 0.2MG BASE/ML)
Approval Date
2002-08-08
Regulatory Status
Discontinued
Drug Name
NALLPEN IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1989-10-31
Active Ingredient
NAFCILLIN SODIUM
Application Number
50655
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/ML
Approval Date
1989-10-31
Regulatory Status
Discontinued
Drug Name
NEXTERONE
Product Number
1
Dosage Form
-
Strength
50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2008-12-24
Active Ingredient
AMIODARONE HYDROCHLORIDE
Application Number
22325
Product Number
1
Dosage Form
-
Strength
50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2008-12-24
Regulatory Status
Discontinued
Drug Name
NOURESS
Product Number
1
Dosage Form
-
Strength
500MG/10ML (50MG/ML)
Approval Date
2019-12-13
Active Ingredient
CYSTEINE HYDROCHLORIDE
Application Number
212535
Product Number
1
Dosage Form
-
Strength
500MG/10ML (50MG/ML)
Approval Date
2019-12-13
Regulatory Status
Discontinued
Drug Name
NOVAMINE 15% SULFITE FREE IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
15% (15GM/100ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-02-05
Active Ingredient
AMINO ACIDS
Application Number
20107
Product Number
1
Dosage Form
-
Strength
15% (15GM/100ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-02-05
Regulatory Status
Discontinued
Drug Name
ONDANSETRON HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE/ML
Approval Date
2013-02-22
Active Ingredient
ONDANSETRON HYDROCHLORIDE
Application Number
78288
Product Number
1
Dosage Form
-
Strength
EQ 2MG BASE/ML
Approval Date
2013-02-22
Regulatory Status
Discontinued
Drug Name
PALONOSETRON HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
EQ 0.25MG BASE/5ML (EQ 0.05MG BASE/ML)
Approval Date
2021-11-12
Active Ingredient
PALONOSETRON HYDROCHLORIDE
Application Number
206916
Product Number
1
Dosage Form
-
Strength
EQ 0.25MG BASE/5ML (EQ 0.05MG BASE/ML)
Approval Date
2021-11-12
Regulatory Status
Discontinued
Drug Name
PEMETREXED DISODIUM
Product Number
1
Dosage Form
-
Strength
EQ 100MG BASE/VIAL
Approval Date
2022-08-18
Active Ingredient
PEMETREXED DISODIUM
Application Number
214436
Product Number
1
Dosage Form
-
Strength
EQ 100MG BASE/VIAL
Approval Date
2022-08-18
Regulatory Status
Discontinued
Drug Name
PEMETREXED DISODIUM
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
2022-08-18
Active Ingredient
PEMETREXED DISODIUM
Application Number
214436
Product Number
2
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
2022-08-18
Regulatory Status
Discontinued
Drug Name
PENTAMIDINE ISETHIONATE
Product Number
1
Dosage Form
-
Strength
300MG/VIAL
Approval Date
1995-12-18
Active Ingredient
PENTAMIDINE ISETHIONATE
Application Number
73617
Product Number
1
Dosage Form
-
Strength
300MG/VIAL
Approval Date
1995-12-18
Regulatory Status
Discontinued
Drug Name
PLASMA-LYTE 148 AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5GM/100ML;30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE
Application Number
17451
Product Number
1
Dosage Form
-
Strength
5GM/100ML;30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PLASMA-LYTE 56 AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5GM/100ML;32MG/100ML;128MG/100ML;234MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; MAGNESIUM ACETATE TETRAHYDRATE; POTASSIUM ACETATE; SODIUM CHLORIDE
Application Number
17385
Product Number
1
Dosage Form
-
Strength
5GM/100ML;32MG/100ML;128MG/100ML;234MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PLASMA-LYTE 56 IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
32MG/100ML;128MG/100ML;234MG/100ML
Approval Date
1984-06-15
Active Ingredient
MAGNESIUM ACETATE TETRAHYDRATE; POTASSIUM ACETATE; SODIUM CHLORIDE
Application Number
19047
Product Number
1
Dosage Form
-
Strength
32MG/100ML;128MG/100ML;234MG/100ML
Approval Date
1984-06-15
Regulatory Status
Discontinued
Drug Name
PLASMA-LYTE M AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
37MG/100ML;5GM/100ML;30MG/100ML;119MG/100ML;161MG/100ML;94MG/100ML;138MG/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM LACTATE
Application Number
17390
Product Number
1
Dosage Form
-
Strength
37MG/100ML;5GM/100ML;30MG/100ML;119MG/100ML;161MG/100ML;94MG/100ML;138MG/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PLASMA-LYTE R IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
36.8MG/100ML;30.5MG/100ML;74.6MG/100ML;640MG/100ML;496MG/100ML;89.6MG/100ML
Approval Date
1982-01-01
Active Ingredient
CALCIUM CHLORIDE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM LACTATE
Application Number
17438
Product Number
1
Dosage Form
-
Strength
36.8MG/100ML;30.5MG/100ML;74.6MG/100ML;640MG/100ML;496MG/100ML;89.6MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE
Product Number
1
Dosage Form
-
Strength
2MEQ/ML
Approval Date
1982-01-01
Active Ingredient
POTASSIUM CHLORIDE
Application Number
80203
Product Number
1
Dosage Form
-
Strength
2MEQ/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE
Product Number
1
Dosage Form
-
Strength
2MEQ/ML
Approval Date
1982-01-01
Active Ingredient
POTASSIUM CHLORIDE
Application Number
85499
Product Number
1
Dosage Form
-
Strength
2MEQ/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE 0.224% IN SODIUM CHLORIDE 0.9%
Product Number
3
Dosage Form
-
Strength
224MG/100ML;900MG/100ML
Approval Date
1982-01-01
Active Ingredient
POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
17648
Product Number
3
Dosage Form
-
Strength
224MG/100ML;900MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE 30MEQ IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
2.24GM/100ML
Approval Date
1989-12-26
Active Ingredient
POTASSIUM CHLORIDE
Application Number
19904
Product Number
3
Dosage Form
-
Strength
2.24GM/100ML
Approval Date
1989-12-26
Regulatory Status
Discontinued
Drug Name
PROCHLORPERAZINE
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
1982-10-01
Active Ingredient
PROCHLORPERAZINE EDISYLATE
Application Number
87759
Product Number
1
Dosage Form
-
Strength
EQ 5MG BASE/ML
Approval Date
1982-10-01
Regulatory Status
Discontinued
Drug Name
PROPRANOLOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
16419
Product Number
1
Dosage Form
-
Strength
1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PROTOPAM CHLORIDE
Product Number
1
Dosage Form
-
Strength
300MG/ML
Approval Date
1982-12-13
Active Ingredient
PRALIDOXIME CHLORIDE
Application Number
18799
Product Number
1
Dosage Form
-
Strength
300MG/ML
Approval Date
1982-12-13
Regulatory Status
Discontinued
Drug Name
RENAMIN W/O ELECTROLYTES
Product Number
7
Dosage Form
-
Strength
6.5% (6.5GM/100ML)
Approval Date
1982-10-15
Active Ingredient
AMINO ACIDS
Application Number
17493
Product Number
7
Dosage Form
-
Strength
6.5% (6.5GM/100ML)
Approval Date
1982-10-15
Regulatory Status
Discontinued
Drug Name
SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
450MG/100ML
Approval Date
1982-01-01
Active Ingredient
SODIUM CHLORIDE
Application Number
17864
Product Number
1
Dosage Form
-
Strength
450MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
450MG/100ML
Approval Date
1982-02-19
Active Ingredient
SODIUM CHLORIDE
Application Number
18497
Product Number
1
Dosage Form
-
Strength
450MG/100ML
Approval Date
1982-02-19
Regulatory Status
Discontinued
Drug Name
SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075%
Product Number
4
Dosage Form
-
Strength
75MG/100ML;900MG/100ML
Approval Date
1982-01-01
Active Ingredient
POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
17648
Product Number
4
Dosage Form
-
Strength
75MG/100ML;900MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
SODIUM HEPARIN
Product Number
1
Dosage Form
-
Strength
1,000 UNITS/ML
Approval Date
1988-03-04
Active Ingredient
HEPARIN SODIUM
Application Number
17036
Product Number
1
Dosage Form
-
Strength
1,000 UNITS/ML
Approval Date
1988-03-04
Regulatory Status
Discontinued
Drug Name
SODIUM LACTATE 0.167 MOLAR IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
1.87GM/100ML
Approval Date
1982-01-01
Active Ingredient
SODIUM LACTATE
Application Number
16692
Product Number
1
Dosage Form
-
Strength
1.87GM/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
SODIUM NITROPRUSSIDE
Product Number
1
Dosage Form
-
Strength
50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-07-28
Active Ingredient
SODIUM NITROPRUSSIDE
Application Number
18581
Product Number
1
Dosage Form
-
Strength
50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-07-28
Regulatory Status
Discontinued
Drug Name
SORBITOL 3% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
3GM/100ML
Approval Date
1982-05-27
Active Ingredient
SORBITOL
Application Number
18512
Product Number
1
Dosage Form
-
Strength
3GM/100ML
Approval Date
1982-05-27
Regulatory Status
Discontinued
Drug Name
SUMATRIPTAN SUCCINATE
Product Number
1
Dosage Form
-
Strength
EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
Approval Date
2023-01-19
Active Ingredient
SUMATRIPTAN SUCCINATE
Application Number
207101
Product Number
1
Dosage Form
-
Strength
EQ 6MG BASE/0.5ML (EQ 12MG BASE/ML)
Approval Date
2023-01-19
Regulatory Status
Discontinued
Drug Name
SYNOVALYTE IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML
Approval Date
1985-01-25
Active Ingredient
MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE
Application Number
19326
Product Number
1
Dosage Form
-
Strength
30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML
Approval Date
1985-01-25
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
40MG/100ML
Approval Date
1982-07-26
Active Ingredient
THEOPHYLLINE
Application Number
18649
Product Number
1
Dosage Form
-
Strength
40MG/100ML
Approval Date
1982-07-26
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
80MG/100ML
Approval Date
1982-07-26
Active Ingredient
THEOPHYLLINE
Application Number
18649
Product Number
2
Dosage Form
-
Strength
80MG/100ML
Approval Date
1982-07-26
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
160MG/100ML
Approval Date
1982-07-26
Active Ingredient
THEOPHYLLINE
Application Number
18649
Product Number
3
Dosage Form
-
Strength
160MG/100ML
Approval Date
1982-07-26
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
200MG/100ML
Approval Date
1982-07-26
Active Ingredient
THEOPHYLLINE
Application Number
18649
Product Number
4
Dosage Form
-
Strength
200MG/100ML
Approval Date
1982-07-26
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
5
Dosage Form
-
Strength
400MG/100ML
Approval Date
1982-07-26
Active Ingredient
THEOPHYLLINE
Application Number
18649
Product Number
5
Dosage Form
-
Strength
400MG/100ML
Approval Date
1982-07-26
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
6
Dosage Form
-
Strength
320MG/100ML
Approval Date
1985-11-13
Active Ingredient
THEOPHYLLINE
Application Number
18649
Product Number
6
Dosage Form
-
Strength
320MG/100ML
Approval Date
1985-11-13
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
7
Dosage Form
-
Strength
4MG/ML
Approval Date
1982-07-26
Active Ingredient
THEOPHYLLINE
Application Number
18649
Product Number
7
Dosage Form
-
Strength
4MG/ML
Approval Date
1982-07-26
Regulatory Status
Discontinued
Drug Name
TRAVAMULSION 10%
Product Number
1
Dosage Form
-
Strength
10%
Approval Date
1982-02-26
Active Ingredient
SOYBEAN OIL
Application Number
18660
Product Number
1
Dosage Form
-
Strength
10%
Approval Date
1982-02-26
Regulatory Status
Discontinued
Drug Name
TRAVAMULSION 20%
Product Number
1
Dosage Form
-
Strength
20%
Approval Date
1983-02-15
Active Ingredient
SOYBEAN OIL
Application Number
18758
Product Number
1
Dosage Form
-
Strength
20%
Approval Date
1983-02-15
Regulatory Status
Discontinued
Drug Name
TRAVASOL 10% W/O ELECTROLYTES
Product Number
6
Dosage Form
-
Strength
10% (10GM/100ML)
Approval Date
1982-01-01
Active Ingredient
AMINO ACIDS
Application Number
17493
Product Number
6
Dosage Form
-
Strength
10% (10GM/100ML)
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TRAVASOL 2.75% IN DEXTROSE 10% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
2.75%;10GM/100ML
Approval Date
1988-09-23
Active Ingredient
AMINO ACIDS; DEXTROSE
Application Number
19520
Product Number
2
Dosage Form
-
Strength
2.75%;10GM/100ML
Approval Date
1988-09-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 2.75% IN DEXTROSE 15% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
2.75%;15GM/100ML
Approval Date
1988-09-23
Active Ingredient
AMINO ACIDS; DEXTROSE
Application Number
19520
Product Number
3
Dosage Form
-
Strength
2.75%;15GM/100ML
Approval Date
1988-09-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 2.75% IN DEXTROSE 20% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
2.75%;20GM/100ML
Approval Date
1988-09-23
Active Ingredient
AMINO ACIDS; DEXTROSE
Application Number
19520
Product Number
4
Dosage Form
-
Strength
2.75%;20GM/100ML
Approval Date
1988-09-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 2.75% IN DEXTROSE 25% IN PLASTIC CONTAINER
Product Number
5
Dosage Form
-
Strength
2.75%;25GM/100ML
Approval Date
1988-09-23
Active Ingredient
AMINO ACIDS; DEXTROSE
Application Number
19520
Product Number
5
Dosage Form
-
Strength
2.75%;25GM/100ML
Approval Date
1988-09-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 2.75% IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
2.75%;5GM/100ML
Approval Date
1988-09-23
Active Ingredient
AMINO ACIDS; DEXTROSE
Application Number
19520
Product Number
1
Dosage Form
-
Strength
2.75%;5GM/100ML
Approval Date
1988-09-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 10% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
2.75%;10GM/100ML;51MG/100ML;261MG/100ML;216MG/100ML;112MG/100ML
Approval Date
1995-10-23
Active Ingredient
AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
20147
Product Number
2
Dosage Form
-
Strength
2.75%;10GM/100ML;51MG/100ML;261MG/100ML;216MG/100ML;112MG/100ML
Approval Date
1995-10-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 15% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
2.75%;15GM/100ML;51MG/100ML;261MG/100ML;216MG/100ML;112MG/100ML
Approval Date
1995-10-23
Active Ingredient
AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
20147
Product Number
3
Dosage Form
-
Strength
2.75%;15GM/100ML;51MG/100ML;261MG/100ML;216MG/100ML;112MG/100ML
Approval Date
1995-10-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 20% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
2.75%;20GM/100ML;51MG/100ML;261MG/100ML;216MG/100ML;112MG/100ML
Approval Date
1995-10-23
Active Ingredient
AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
20147
Product Number
4
Dosage Form
-
Strength
2.75%;20GM/100ML;51MG/100ML;261MG/100ML;216MG/100ML;112MG/100ML
Approval Date
1995-10-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 25% IN PLASTIC CONTAINER
Product Number
5
Dosage Form
-
Strength
2.75%;25GM/100ML;51MG/100ML;261MG/100ML;216MG/100ML;112MG/100ML
Approval Date
1995-10-23
Active Ingredient
AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
20147
Product Number
5
Dosage Form
-
Strength
2.75%;25GM/100ML;51MG/100ML;261MG/100ML;216MG/100ML;112MG/100ML
Approval Date
1995-10-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
2.75%;5GM/100ML;51MG/100ML;261MG/100ML;216MG/100ML;112MG/100ML
Approval Date
1995-10-23
Active Ingredient
AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
20147
Product Number
1
Dosage Form
-
Strength
2.75%;5GM/100ML;51MG/100ML;261MG/100ML;216MG/100ML;112MG/100ML
Approval Date
1995-10-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 3.5% SULFITE FREE W/ ELECTROLYTES IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
3.5%;51MG/100ML;131MG/100ML;218MG/100ML;35MG/100ML
Approval Date
1995-10-23
Active Ingredient
AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
20177
Product Number
1
Dosage Form
-
Strength
3.5%;51MG/100ML;131MG/100ML;218MG/100ML;35MG/100ML
Approval Date
1995-10-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 3.5% W/ ELECTROLYTES
Product Number
3
Dosage Form
-
Strength
3.5%;51MG/100ML;131MG/100ML;218MG/100ML;35MG/100ML
Approval Date
1982-01-01
Active Ingredient
AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
17493
Product Number
3
Dosage Form
-
Strength
3.5%;51MG/100ML;131MG/100ML;218MG/100ML;35MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TRAVASOL 4.25% IN DEXTROSE 10% IN PLASTIC CONTAINER
Product Number
7
Dosage Form
-
Strength
4.25%;10GM/100ML
Approval Date
1988-09-23
Active Ingredient
AMINO ACIDS; DEXTROSE
Application Number
19520
Product Number
7
Dosage Form
-
Strength
4.25%;10GM/100ML
Approval Date
1988-09-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 4.25% IN DEXTROSE 15% IN PLASTIC CONTAINER
Product Number
8
Dosage Form
-
Strength
4.25%;15GM/100ML
Approval Date
1988-09-23
Active Ingredient
AMINO ACIDS; DEXTROSE
Application Number
19520
Product Number
8
Dosage Form
-
Strength
4.25%;15GM/100ML
Approval Date
1988-09-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER
Product Number
9
Dosage Form
-
Strength
4.25%;20GM/100ML
Approval Date
1988-09-23
Active Ingredient
AMINO ACIDS; DEXTROSE
Application Number
19520
Product Number
9
Dosage Form
-
Strength
4.25%;20GM/100ML
Approval Date
1988-09-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 4.25% IN DEXTROSE 25% IN PLASTIC CONTAINER
Product Number
10
Dosage Form
-
Strength
4.25%;25GM/100ML
Approval Date
1988-09-23
Active Ingredient
AMINO ACIDS; DEXTROSE
Application Number
19520
Product Number
10
Dosage Form
-
Strength
4.25%;25GM/100ML
Approval Date
1988-09-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 4.25% IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
6
Dosage Form
-
Strength
4.25%;5GM/100ML
Approval Date
1988-09-23
Active Ingredient
AMINO ACIDS; DEXTROSE
Application Number
19520
Product Number
6
Dosage Form
-
Strength
4.25%;5GM/100ML
Approval Date
1988-09-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 4.25% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 10% IN PLASTIC CONTAINER
Product Number
7
Dosage Form
-
Strength
4.25%;10GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML
Approval Date
1995-10-23
Active Ingredient
AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
20147
Product Number
7
Dosage Form
-
Strength
4.25%;10GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML
Approval Date
1995-10-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 4.25% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 15% IN PLASTIC CONTAINER
Product Number
8
Dosage Form
-
Strength
4.25%;15GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML
Approval Date
1995-10-23
Active Ingredient
AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
20147
Product Number
8
Dosage Form
-
Strength
4.25%;15GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML
Approval Date
1995-10-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 4.25% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 20% IN PLASTIC CONTAINER
Product Number
9
Dosage Form
-
Strength
4.25%;20GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML
Approval Date
1995-10-23
Active Ingredient
AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
20147
Product Number
9
Dosage Form
-
Strength
4.25%;20GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML
Approval Date
1995-10-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 4.25% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 25% IN PLASTIC CONTAINER
Product Number
10
Dosage Form
-
Strength
4.25%;25GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML
Approval Date
1995-10-23
Active Ingredient
AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
20147
Product Number
10
Dosage Form
-
Strength
4.25%;25GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML
Approval Date
1995-10-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 4.25% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
6
Dosage Form
-
Strength
4.25%;5GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML
Approval Date
1995-10-23
Active Ingredient
AMINO ACIDS; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
20147
Product Number
6
Dosage Form
-
Strength
4.25%;5GM/100ML;51MG/100ML;261MG/100ML;297MG/100ML;77MG/100ML
Approval Date
1995-10-23
Regulatory Status
Discontinued
Drug Name
TRAVASOL 5.5% SULFITE FREE W/ ELECTROLYTES IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5.5%;102MG/100ML;522MG/100ML;431MG/100ML;224MG/100ML
Approval Date
1995-10-27
Active Ingredient
AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
20173
Product Number
1
Dosage Form
-
Strength
5.5%;102MG/100ML;522MG/100ML;431MG/100ML;224MG/100ML
Approval Date
1995-10-27
Regulatory Status
Discontinued
Drug Name
TRAVASOL 5.5% W/ ELECTROLYTES
Product Number
1
Dosage Form
-
Strength
5.5%;102MG/100ML;522MG/100ML;431MG/100ML;224MG/100ML
Approval Date
1982-01-01
Active Ingredient
AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
17493
Product Number
1
Dosage Form
-
Strength
5.5%;102MG/100ML;522MG/100ML;431MG/100ML;224MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TRAVASOL 5.5% W/O ELECTROLYTES
Product Number
4
Dosage Form
-
Strength
5.5% (5.5GM/100ML)
Approval Date
1982-01-01
Active Ingredient
AMINO ACIDS
Application Number
17493
Product Number
4
Dosage Form
-
Strength
5.5% (5.5GM/100ML)
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TRAVASOL 8.5% SULFITE FREE W/ ELECTROLYTES IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
8.5%;102MG/100ML;522MG/100ML;594MG/100ML;154MG/100ML
Approval Date
1995-10-27
Active Ingredient
AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
20173
Product Number
2
Dosage Form
-
Strength
8.5%;102MG/100ML;522MG/100ML;594MG/100ML;154MG/100ML
Approval Date
1995-10-27
Regulatory Status
Discontinued
Drug Name
TRAVASOL 8.5% W/ ELECTROLYTES
Product Number
2
Dosage Form
-
Strength
8.5%;102MG/100ML;522MG/100ML;594MG/100ML;154MG/100ML
Approval Date
1982-01-01
Active Ingredient
AMINO ACIDS; MAGNESIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
17493
Product Number
2
Dosage Form
-
Strength
8.5%;102MG/100ML;522MG/100ML;594MG/100ML;154MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TRAVASOL 8.5% W/O ELECTROLYTES
Product Number
5
Dosage Form
-
Strength
8.5% (8.5GM/100ML)
Approval Date
1982-01-01
Active Ingredient
AMINO ACIDS
Application Number
17493
Product Number
5
Dosage Form
-
Strength
8.5% (8.5GM/100ML)
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TRAVERT 10% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
10GM/100ML
Approval Date
1982-01-01
Active Ingredient
INVERT SUGAR
Application Number
16717
Product Number
1
Dosage Form
-
Strength
10GM/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
WYAMINE SULFATE
Product Number
1
Dosage Form
-
Strength
EQ 30MG BASE/ML
Approval Date
1982-01-01
Active Ingredient
MEPHENTERMINE SULFATE
Application Number
8248
Product Number
1
Dosage Form
-
Strength
EQ 30MG BASE/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
WYAMINE SULFATE
Product Number
2
Dosage Form
-
Strength
EQ 15MG BASE/ML
Approval Date
1982-01-01
Active Ingredient
MEPHENTERMINE SULFATE
Application Number
8248
Product Number
2
Dosage Form
-
Strength
EQ 15MG BASE/ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Status Breakdown
212 total- Discontinued
Official Source
FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.
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Drug Name
AMINOCAPROIC ACID
Application Number
18590
Product Number
1
Active Ingredient
AMINOCAPROIC ACID
Dosage Form
-
Strength
250MG/ML
FDA Approved Drug Data
Approved drug product information
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Data maintained from official sources
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