B. Braun Medical Discontinued
FDA Approved Drugs
B. Braun Medical 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 167
- Latest Approval Date Jun 13, 2011
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Overview
Social Profiles
Company Snapshot
B. Braun Medical Discontinued
824 Twelfth Avenue Bethlehem, PA 18018-3524
U.S.A
www.bbraunusa.com/en.html View on MapFDA Approved Drug Records ( 167 records )
Drug Name
ACETATED RINGERS IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
20MG/100ML;30MG/100ML;380MG/100ML;600MG/100ML
Approval Date
1982-11-29
Active Ingredient
CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
18725
Product Number
1
Dosage Form
-
Strength
20MG/100ML;30MG/100ML;380MG/100ML;600MG/100ML
Approval Date
1982-11-29
Regulatory Status
Discontinued
Drug Name
AMMONIUM CHLORIDE 2.14%
Product Number
1
Dosage Form
-
Strength
40MEQ/100ML
Approval Date
1982-01-01
Active Ingredient
AMMONIUM CHLORIDE
Application Number
85734
Product Number
1
Dosage Form
-
Strength
40MEQ/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
BRETYLIUM TOSYLATE IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
100MG/100ML
Approval Date
1986-04-29
Active Ingredient
BRETYLIUM TOSYLATE
Application Number
19121
Product Number
1
Dosage Form
-
Strength
100MG/100ML
Approval Date
1986-04-29
Regulatory Status
Discontinued
Drug Name
BRETYLIUM TOSYLATE IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
200MG/100ML
Approval Date
1986-04-29
Active Ingredient
BRETYLIUM TOSYLATE
Application Number
19121
Product Number
2
Dosage Form
-
Strength
200MG/100ML
Approval Date
1986-04-29
Regulatory Status
Discontinued
Drug Name
BRETYLIUM TOSYLATE IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
400MG/100ML
Approval Date
1986-04-29
Active Ingredient
BRETYLIUM TOSYLATE
Application Number
19121
Product Number
3
Dosage Form
-
Strength
400MG/100ML
Approval Date
1986-04-29
Regulatory Status
Discontinued
Drug Name
CEFAZOLIN AND DEXTROSE
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
2000-07-27
Active Ingredient
CEFAZOLIN SODIUM
Application Number
50779
Product Number
1
Dosage Form
-
Strength
EQ 500MG BASE/VIAL
Approval Date
2000-07-27
Regulatory Status
Discontinued
Drug Name
CEFOTAXIME AND DEXTROSE 2.4% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
EQ 2GM BASE
Approval Date
2004-07-29
Active Ingredient
CEFOTAXIME SODIUM
Application Number
50792
Product Number
1
Dosage Form
-
Strength
EQ 2GM BASE
Approval Date
2004-07-29
Regulatory Status
Discontinued
Drug Name
CEFOTAXIME AND DEXTROSE 3.9% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
EQ 1GM BASE
Approval Date
2004-07-29
Active Ingredient
CEFOTAXIME SODIUM
Application Number
50792
Product Number
2
Dosage Form
-
Strength
EQ 1GM BASE
Approval Date
2004-07-29
Regulatory Status
Discontinued
Drug Name
CEFOTETAN AND DEXTROSE IN DUPLEX CONTAINER
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2007-08-09
Active Ingredient
CEFOTETAN DISODIUM
Application Number
65430
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE/VIAL
Approval Date
2007-08-09
Regulatory Status
Discontinued
Drug Name
CEFOTETAN AND DEXTROSE IN DUPLEX CONTAINER
Product Number
2
Dosage Form
-
Strength
EQ 2GM BASE/VIAL
Approval Date
2007-08-09
Active Ingredient
CEFOTETAN DISODIUM
Application Number
65430
Product Number
2
Dosage Form
-
Strength
EQ 2GM BASE/VIAL
Approval Date
2007-08-09
Regulatory Status
Discontinued
Drug Name
CEFTAZIDIME IN DEXTROSE CONTAINER
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE
Approval Date
2011-06-13
Active Ingredient
CEFTAZIDIME
Application Number
50823
Product Number
1
Dosage Form
-
Strength
EQ 1GM BASE
Approval Date
2011-06-13
Regulatory Status
Discontinued
Drug Name
CEFTAZIDIME IN DEXTROSE CONTAINER
Product Number
2
Dosage Form
-
Strength
EQ 2GM BASE
Approval Date
2011-06-13
Active Ingredient
CEFTAZIDIME
Application Number
50823
Product Number
2
Dosage Form
-
Strength
EQ 2GM BASE
Approval Date
2011-06-13
Regulatory Status
Discontinued
Drug Name
CEFUROXIME AND DEXTROSE IN DUPLEX CONTAINER
Product Number
1
Dosage Form
-
Strength
EQ 750MG BASE/VIAL
Approval Date
2001-02-21
Active Ingredient
CEFUROXIME SODIUM
Application Number
50780
Product Number
1
Dosage Form
-
Strength
EQ 750MG BASE/VIAL
Approval Date
2001-02-21
Regulatory Status
Discontinued
Drug Name
CEFUROXIME AND DEXTROSE IN DUPLEX CONTAINER
Product Number
2
Dosage Form
-
Strength
EQ 1.5GM BASE/VIAL
Approval Date
2001-02-21
Active Ingredient
CEFUROXIME SODIUM
Application Number
50780
Product Number
2
Dosage Form
-
Strength
EQ 1.5GM BASE/VIAL
Approval Date
2001-02-21
Regulatory Status
Discontinued
Drug Name
DEXTROSE 10% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
10GM/100ML;200MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; SODIUM CHLORIDE
Application Number
18386
Product Number
1
Dosage Form
-
Strength
10GM/100ML;200MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 10% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
10GM/100ML;450MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; SODIUM CHLORIDE
Application Number
18229
Product Number
1
Dosage Form
-
Strength
10GM/100ML;450MG/100ML
Approval Date
1982-01-01
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
18047
Product Number
1
Dosage Form
-
Strength
10GM/100ML;900MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 10% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
10GM/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE
Application Number
18046
Product Number
1
Dosage Form
-
Strength
10GM/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 2.5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
2.5GM/100ML;450MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; SODIUM CHLORIDE
Application Number
18030
Product Number
1
Dosage Form
-
Strength
2.5GM/100ML;450MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 2.5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
2.5GM/100ML;900MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; SODIUM CHLORIDE
Application Number
18376
Product Number
1
Dosage Form
-
Strength
2.5GM/100ML;900MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 2.5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
2.5GM/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE
Application Number
18358
Product Number
1
Dosage Form
-
Strength
2.5GM/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 2.5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
2.5GM/100ML
Approval Date
1988-02-02
Active Ingredient
DEXTROSE
Application Number
19626
Product Number
1
Dosage Form
-
Strength
2.5GM/100ML
Approval Date
1988-02-02
Regulatory Status
Discontinued
Drug Name
DEXTROSE 4% IN MODIFIED LACTATED RINGERS IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
4MG/100ML;4GM/100ML;6MG/100ML;120MG/100ML;62MG/100ML
Approval Date
1988-02-24
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Application Number
19634
Product Number
2
Dosage Form
-
Strength
4MG/100ML;4GM/100ML;6MG/100ML;120MG/100ML;62MG/100ML
Approval Date
1988-02-24
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER
Product Number
5
Dosage Form
-
Strength
5GM/100ML;110MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; SODIUM CHLORIDE
Application Number
18030
Product Number
5
Dosage Form
-
Strength
5GM/100ML;110MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
5GM/100ML;200MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; SODIUM CHLORIDE
Application Number
18030
Product Number
4
Dosage Form
-
Strength
5GM/100ML;200MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5% AND SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
5GM/100ML;330MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; SODIUM CHLORIDE
Application Number
18030
Product Number
3
Dosage Form
-
Strength
5GM/100ML;330MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
5GM/100ML;450MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; SODIUM CHLORIDE
Application Number
18030
Product Number
2
Dosage Form
-
Strength
5GM/100ML;450MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5GM/100ML;900MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; SODIUM CHLORIDE
Application Number
18026
Product Number
1
Dosage Form
-
Strength
5GM/100ML;900MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5% IN ACETATED RINGERS IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
20MG/100ML;5GM/100ML;30MG/100ML;380MG/100ML;600MG/100ML
Approval Date
1982-01-01
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
18258
Product Number
1
Dosage Form
-
Strength
20MG/100ML;5GM/100ML;30MG/100ML;380MG/100ML;600MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5% IN LACTATED RINGERS IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
20MG/100ML;5GM/100ML;30MG/100ML;600MG/100ML;310MG/100ML
Approval Date
1982-01-01
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Application Number
17510
Product Number
1
Dosage Form
-
Strength
20MG/100ML;5GM/100ML;30MG/100ML;600MG/100ML;310MG/100ML
Approval Date
1982-01-01
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
18256
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% IN RINGERS IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
33MG/100ML;5GM/100ML;30MG/100ML;860MG/100ML
Approval Date
1992-04-17
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
20000
Product Number
1
Dosage Form
-
Strength
33MG/100ML;5GM/100ML;30MG/100ML;860MG/100ML
Approval Date
1992-04-17
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 0.075%
Product Number
9
Dosage Form
-
Strength
5GM/100ML;75MG/100ML;200MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18268
Product Number
9
Dosage Form
-
Strength
5GM/100ML;75MG/100ML;200MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 0.15% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
5GM/100ML;150MG/100ML;200MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18268
Product Number
4
Dosage Form
-
Strength
5GM/100ML;150MG/100ML;200MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 0.224% IN PLASTIC CONTAINER
Product Number
5
Dosage Form
-
Strength
5GM/100ML;220MG/100ML;200MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18268
Product Number
5
Dosage Form
-
Strength
5GM/100ML;220MG/100ML;200MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5%, SODIUM CHLORIDE 0.2% AND POTASSIUM CHLORIDE 0.3% IN PLASTIC CONTAINER
Product Number
6
Dosage Form
-
Strength
5GM/100ML;300MG/100ML;200MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18268
Product Number
6
Dosage Form
-
Strength
5GM/100ML;300MG/100ML;200MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 0.075% IN PLASTIC CONTAINER
Product Number
11
Dosage Form
-
Strength
5GM/100ML;75MG/100ML;330MG/100ML
Approval Date
1986-01-18
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18268
Product Number
11
Dosage Form
-
Strength
5GM/100ML;75MG/100ML;330MG/100ML
Approval Date
1986-01-18
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 0.15% IN PLASTIC CONTAINER
Product Number
12
Dosage Form
-
Strength
5GM/100ML;150MG/100ML;330MG/100ML
Approval Date
1986-01-18
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18268
Product Number
12
Dosage Form
-
Strength
5GM/100ML;150MG/100ML;330MG/100ML
Approval Date
1986-01-18
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 0.22% IN PLASTIC CONTAINER
Product Number
13
Dosage Form
-
Strength
5GM/100ML;220MG/100ML;330MG/100ML
Approval Date
1986-01-18
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18268
Product Number
13
Dosage Form
-
Strength
5GM/100ML;220MG/100ML;330MG/100ML
Approval Date
1986-01-18
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5%, SODIUM CHLORIDE 0.33% AND POTASSIUM CHLORIDE 0.30% IN PLASTIC CONTAINER
Product Number
14
Dosage Form
-
Strength
5GM/100ML;300MG/100ML;330MG/100ML
Approval Date
1986-01-18
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18268
Product Number
14
Dosage Form
-
Strength
5GM/100ML;300MG/100ML;330MG/100ML
Approval Date
1986-01-18
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5%, SODIUM CHLORIDE 0.45% AND POTASSIUM CHLORIDE 0.075%
Product Number
10
Dosage Form
-
Strength
5GM/100ML;75MG/100ML;450MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18268
Product Number
10
Dosage Form
-
Strength
5GM/100ML;75MG/100ML;450MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5%, SODIUM CHLORIDE 0.45% AND POTASSIUM CHLORIDE 0.15% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5GM/100ML;150MG/100ML;450MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18268
Product Number
1
Dosage Form
-
Strength
5GM/100ML;150MG/100ML;450MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5%, SODIUM CHLORIDE 0.45% AND POTASSIUM CHLORIDE 0.22% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
5GM/100ML;220MG/100ML;450MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18268
Product Number
2
Dosage Form
-
Strength
5GM/100ML;220MG/100ML;450MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 5%, SODIUM CHLORIDE 0.45% AND POTASSIUM CHLORIDE 0.3% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
5GM/100ML;300MG/100ML;450MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18268
Product Number
3
Dosage Form
-
Strength
5GM/100ML;300MG/100ML;450MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 60%
Product Number
2
Dosage Form
-
Strength
60GM/100ML
Approval Date
1982-09-22
Active Ingredient
DEXTROSE
Application Number
17995
Product Number
2
Dosage Form
-
Strength
60GM/100ML
Approval Date
1982-09-22
Regulatory Status
Discontinued
Drug Name
DEXTROSE 60% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
60GM/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE
Application Number
17995
Product Number
1
Dosage Form
-
Strength
60GM/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DEXTROSE 7.7% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
7.7GM/100ML
Approval Date
1988-02-02
Active Ingredient
DEXTROSE
Application Number
19626
Product Number
3
Dosage Form
-
Strength
7.7GM/100ML
Approval Date
1988-02-02
Regulatory Status
Discontinued
Drug Name
DIALYTE CONCENTRATE W/ DEXTROSE 30% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
510MG/100ML;30GM/100ML;200MG/100ML;9.2GM/100ML;9.6GM/100ML
Approval Date
1983-08-26
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
18807
Product Number
1
Dosage Form
-
Strength
510MG/100ML;30GM/100ML;200MG/100ML;9.2GM/100ML;9.6GM/100ML
Approval Date
1983-08-26
Regulatory Status
Discontinued
Drug Name
DIALYTE CONCENTRATE W/ DEXTROSE 30% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
510MG/100ML;30GM/100ML;200MG/100ML;9.4GM/100ML;11GM/100ML
Approval Date
1983-08-26
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
18807
Product Number
3
Dosage Form
-
Strength
510MG/100ML;30GM/100ML;200MG/100ML;9.4GM/100ML;11GM/100ML
Approval Date
1983-08-26
Regulatory Status
Discontinued
Drug Name
DIALYTE CONCENTRATE W/ DEXTROSE 50% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
510MG/100ML;50GM/100ML;200MG/100ML;9.2GM/100ML;9.6GM/100ML
Approval Date
1983-08-26
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
18807
Product Number
2
Dosage Form
-
Strength
510MG/100ML;50GM/100ML;200MG/100ML;9.2GM/100ML;9.6GM/100ML
Approval Date
1983-08-26
Regulatory Status
Discontinued
Drug Name
DIALYTE CONCENTRATE W/ DEXTROSE 50% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
510MG/100ML;50GM/100ML;200MG/100ML;9.4GM/100ML;11GM/100ML
Approval Date
1983-08-26
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
18807
Product Number
4
Dosage Form
-
Strength
510MG/100ML;50GM/100ML;200MG/100ML;9.4GM/100ML;11GM/100ML
Approval Date
1983-08-26
Regulatory Status
Discontinued
Drug Name
DIALYTE LM/ DEXTROSE 1.5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
26MG/100ML;1.5GM/100ML;15MG/100ML;560MG/100ML;390MG/100ML
Approval Date
1982-01-01
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Application Number
18460
Product Number
2
Dosage Form
-
Strength
26MG/100ML;1.5GM/100ML;15MG/100ML;560MG/100ML;390MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DIALYTE LM/ DEXTROSE 1.5% IN PLASTIC CONTAINER
Product Number
7
Dosage Form
-
Strength
26MG/100ML;1.5GM/100ML;5MG/100ML;530MG/100ML;450MG/100ML
Approval Date
1986-01-29
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Application Number
18460
Product Number
7
Dosage Form
-
Strength
26MG/100ML;1.5GM/100ML;5MG/100ML;530MG/100ML;450MG/100ML
Approval Date
1986-01-29
Regulatory Status
Discontinued
Drug Name
DIALYTE LM/ DEXTROSE 2.5% IN PLASTIC CONTAINER
Product Number
5
Dosage Form
-
Strength
26MG/100ML;2.5GM/100ML;5MG/100ML;530MG/100ML;450MG/100ML
Approval Date
1983-11-02
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Application Number
18460
Product Number
5
Dosage Form
-
Strength
26MG/100ML;2.5GM/100ML;5MG/100ML;530MG/100ML;450MG/100ML
Approval Date
1983-11-02
Regulatory Status
Discontinued
Drug Name
DIALYTE LM/ DEXTROSE 2.5% IN PLASTIC CONTAINER
Product Number
6
Dosage Form
-
Strength
29MG/100ML;2.5GM/100ML;15MG/100ML;610MG/100ML;560MG/100ML
Approval Date
1986-01-29
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
18460
Product Number
6
Dosage Form
-
Strength
29MG/100ML;2.5GM/100ML;15MG/100ML;610MG/100ML;560MG/100ML
Approval Date
1986-01-29
Regulatory Status
Discontinued
Drug Name
DIALYTE LM/ DEXTROSE 2.5% IN PLASTIC CONTAINER
Product Number
8
Dosage Form
-
Strength
26MG/100ML;5GM/100ML;5MG/100ML;530MG/100ML;450MG/100ML
Approval Date
1986-01-29
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Application Number
18460
Product Number
8
Dosage Form
-
Strength
26MG/100ML;5GM/100ML;5MG/100ML;530MG/100ML;450MG/100ML
Approval Date
1986-01-29
Regulatory Status
Discontinued
Drug Name
DIALYTE LM/ DEXTROSE 4.25% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
26MG/100ML;4.25GM/100ML;15MG/100ML;560MG/100ML;390MG/100ML
Approval Date
1982-01-01
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Application Number
18460
Product Number
4
Dosage Form
-
Strength
26MG/100ML;4.25GM/100ML;15MG/100ML;560MG/100ML;390MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DIALYTE LM/ DEXTROSE 4.25% IN PLASTIC CONTAINER
Product Number
9
Dosage Form
-
Strength
26MG/100ML;4.25GM/100ML;5MG/100ML;530MG/100ML;450MG/100ML
Approval Date
1986-01-29
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Application Number
18460
Product Number
9
Dosage Form
-
Strength
26MG/100ML;4.25GM/100ML;5MG/100ML;530MG/100ML;450MG/100ML
Approval Date
1986-01-29
Regulatory Status
Discontinued
Drug Name
DIALYTE W/ DEXTROSE 1.5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
29MG/100ML;1.5GM/100ML;15MG/100ML;610MG/100ML;560MG/100ML
Approval Date
1982-01-01
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
18460
Product Number
1
Dosage Form
-
Strength
29MG/100ML;1.5GM/100ML;15MG/100ML;610MG/100ML;560MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DIALYTE W/ DEXTROSE 4.25% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
29MG/100ML;4.25GM/100ML;15MG/100ML;610MG/100ML;560MG/100ML
Approval Date
1982-01-01
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
18460
Product Number
3
Dosage Form
-
Strength
29MG/100ML;4.25GM/100ML;15MG/100ML;610MG/100ML;560MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
DOPAMINE HYDROCHLORIDE AND DEXTROSE 5%
Product Number
2
Dosage Form
-
Strength
80MG/100ML
Approval Date
1986-10-15
Active Ingredient
DOPAMINE HYDROCHLORIDE
Application Number
19099
Product Number
2
Dosage Form
-
Strength
80MG/100ML
Approval Date
1986-10-15
Regulatory Status
Discontinued
Drug Name
DOPAMINE HYDROCHLORIDE AND DEXTROSE 5%
Product Number
4
Dosage Form
-
Strength
320MG/100ML
Approval Date
1986-10-15
Active Ingredient
DOPAMINE HYDROCHLORIDE
Application Number
19099
Product Number
4
Dosage Form
-
Strength
320MG/100ML
Approval Date
1986-10-15
Regulatory Status
Discontinued
Drug Name
DOPAMINE HYDROCHLORIDE AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
40MG/100ML
Approval Date
1986-10-15
Active Ingredient
DOPAMINE HYDROCHLORIDE
Application Number
19099
Product Number
1
Dosage Form
-
Strength
40MG/100ML
Approval Date
1986-10-15
Regulatory Status
Discontinued
Drug Name
DOPAMINE HYDROCHLORIDE AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
160MG/100ML
Approval Date
1986-10-15
Active Ingredient
DOPAMINE HYDROCHLORIDE
Application Number
19099
Product Number
3
Dosage Form
-
Strength
160MG/100ML
Approval Date
1986-10-15
Regulatory Status
Discontinued
Drug Name
FREAMINE 8.5%
Product Number
1
Dosage Form
-
Strength
8.5% (8.5GM/100ML)
Approval Date
1982-01-01
Active Ingredient
AMINO ACIDS
Application Number
16822
Product Number
1
Dosage Form
-
Strength
8.5% (8.5GM/100ML)
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
FREAMINE HBC 6.9%
Product Number
6
Dosage Form
-
Strength
6.9% (6.9GM/100ML)
Approval Date
1983-05-17
Active Ingredient
AMINO ACIDS
Application Number
16822
Product Number
6
Dosage Form
-
Strength
6.9% (6.9GM/100ML)
Approval Date
1983-05-17
Regulatory Status
Discontinued
Drug Name
FREAMINE II 8.5%
Product Number
2
Dosage Form
-
Strength
8.5% (8.5GM/100ML)
Approval Date
1982-01-01
Active Ingredient
AMINO ACIDS
Application Number
16822
Product Number
2
Dosage Form
-
Strength
8.5% (8.5GM/100ML)
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
FREAMINE III 10%
Product Number
5
Dosage Form
-
Strength
10% (10GM/100ML)
Approval Date
1982-01-01
Active Ingredient
AMINO ACIDS
Application Number
16822
Product Number
5
Dosage Form
-
Strength
10% (10GM/100ML)
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
FREAMINE III 3% W/ ELECTROLYTES
Product Number
3
Dosage Form
-
Strength
3%;54MG/100ML;40MG/100ML;150MG/100ML;200MG/100ML;120MG/100ML
Approval Date
1982-01-01
Active Ingredient
AMINO ACIDS; MAGNESIUM ACETATE; PHOSPHORIC ACID; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
16822
Product Number
3
Dosage Form
-
Strength
3%;54MG/100ML;40MG/100ML;150MG/100ML;200MG/100ML;120MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
FREAMINE III 8.5%
Product Number
4
Dosage Form
-
Strength
8.5% (8.5GM/100ML)
Approval Date
1982-01-01
Active Ingredient
AMINO ACIDS
Application Number
16822
Product Number
4
Dosage Form
-
Strength
8.5% (8.5GM/100ML)
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
FREAMINE III 8.5% W/ ELECTROLYTES
Product Number
7
Dosage Form
-
Strength
8.5%;110MG/100ML;230MG/100ML;10MG/100ML;440MG/100ML;690MG/100ML
Approval Date
1988-07-01
Active Ingredient
AMINO ACIDS; MAGNESIUM ACETATE; PHOSPHORIC ACID; POTASSIUM ACETATE; POTASSIUM CHLORIDE; SODIUM ACETATE
Application Number
16822
Product Number
7
Dosage Form
-
Strength
8.5%;110MG/100ML;230MG/100ML;10MG/100ML;440MG/100ML;690MG/100ML
Approval Date
1988-07-01
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
1987-08-28
Active Ingredient
GENTAMICIN SULFATE
Application Number
62814
Product Number
1
Dosage Form
-
Strength
EQ 0.8MG BASE/ML
Approval Date
1987-08-28
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
EQ 1.2MG BASE/ML
Approval Date
1987-08-28
Active Ingredient
GENTAMICIN SULFATE
Application Number
62814
Product Number
2
Dosage Form
-
Strength
EQ 1.2MG BASE/ML
Approval Date
1987-08-28
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
EQ 1.4MG BASE/ML
Approval Date
1987-08-28
Active Ingredient
GENTAMICIN SULFATE
Application Number
62814
Product Number
3
Dosage Form
-
Strength
EQ 1.4MG BASE/ML
Approval Date
1987-08-28
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
EQ 1.6MG BASE/ML
Approval Date
1987-08-28
Active Ingredient
GENTAMICIN SULFATE
Application Number
62814
Product Number
4
Dosage Form
-
Strength
EQ 1.6MG BASE/ML
Approval Date
1987-08-28
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
5
Dosage Form
-
Strength
EQ 1.8MG BASE/ML
Approval Date
1987-08-28
Active Ingredient
GENTAMICIN SULFATE
Application Number
62814
Product Number
5
Dosage Form
-
Strength
EQ 1.8MG BASE/ML
Approval Date
1987-08-28
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
6
Dosage Form
-
Strength
EQ 2MG BASE/ML
Approval Date
1987-08-28
Active Ingredient
GENTAMICIN SULFATE
Application Number
62814
Product Number
6
Dosage Form
-
Strength
EQ 2MG BASE/ML
Approval Date
1987-08-28
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
7
Dosage Form
-
Strength
EQ 2.4MG BASE/ML
Approval Date
1987-08-28
Active Ingredient
GENTAMICIN SULFATE
Application Number
62814
Product Number
7
Dosage Form
-
Strength
EQ 2.4MG BASE/ML
Approval Date
1987-08-28
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
8
Dosage Form
-
Strength
EQ 40MG BASE/100ML
Approval Date
1987-08-28
Active Ingredient
GENTAMICIN SULFATE
Application Number
62814
Product Number
8
Dosage Form
-
Strength
EQ 40MG BASE/100ML
Approval Date
1987-08-28
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
9
Dosage Form
-
Strength
EQ 60MG BASE/100ML
Approval Date
1987-08-28
Active Ingredient
GENTAMICIN SULFATE
Application Number
62814
Product Number
9
Dosage Form
-
Strength
EQ 60MG BASE/100ML
Approval Date
1987-08-28
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
10
Dosage Form
-
Strength
EQ 70MG BASE/100ML
Approval Date
1987-08-28
Active Ingredient
GENTAMICIN SULFATE
Application Number
62814
Product Number
10
Dosage Form
-
Strength
EQ 70MG BASE/100ML
Approval Date
1987-08-28
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
11
Dosage Form
-
Strength
EQ 80MG BASE/100ML
Approval Date
1987-08-28
Active Ingredient
GENTAMICIN SULFATE
Application Number
62814
Product Number
11
Dosage Form
-
Strength
EQ 80MG BASE/100ML
Approval Date
1987-08-28
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
12
Dosage Form
-
Strength
EQ 90MG BASE/100ML
Approval Date
1987-08-28
Active Ingredient
GENTAMICIN SULFATE
Application Number
62814
Product Number
12
Dosage Form
-
Strength
EQ 90MG BASE/100ML
Approval Date
1987-08-28
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
13
Dosage Form
-
Strength
EQ 100MG BASE/100ML
Approval Date
1987-08-28
Active Ingredient
GENTAMICIN SULFATE
Application Number
62814
Product Number
13
Dosage Form
-
Strength
EQ 100MG BASE/100ML
Approval Date
1987-08-28
Regulatory Status
Discontinued
Drug Name
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
14
Dosage Form
-
Strength
EQ 120MG BASE/100ML
Approval Date
1987-08-28
Active Ingredient
GENTAMICIN SULFATE
Application Number
62814
Product Number
14
Dosage Form
-
Strength
EQ 120MG BASE/100ML
Approval Date
1987-08-28
Regulatory Status
Discontinued
Drug Name
HEPARIN SODIUM 1,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
200 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-03-29
Active Ingredient
HEPARIN SODIUM
Application Number
19042
Product Number
1
Dosage Form
-
Strength
200 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-03-29
Regulatory Status
Discontinued
Drug Name
HEPARIN SODIUM 12,500 UNITS IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1992-07-20
Active Ingredient
HEPARIN SODIUM
Application Number
19802
Product Number
1
Dosage Form
-
Strength
5,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1992-07-20
Regulatory Status
Discontinued
Drug Name
HEPARIN SODIUM 2,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
200 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-03-29
Active Ingredient
HEPARIN SODIUM
Application Number
19042
Product Number
2
Dosage Form
-
Strength
200 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-03-29
Regulatory Status
Discontinued
Drug Name
HEPARIN SODIUM 25,000 UNITS IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5,000 UNITS/100ML
Approval Date
1985-03-29
Active Ingredient
HEPARIN SODIUM
Application Number
19134
Product Number
1
Dosage Form
-
Strength
5,000 UNITS/100ML
Approval Date
1985-03-29
Regulatory Status
Discontinued
Drug Name
HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
10,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1992-07-20
Active Ingredient
HEPARIN SODIUM
Application Number
19802
Product Number
2
Dosage Form
-
Strength
10,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1992-07-20
Regulatory Status
Discontinued
Drug Name
HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
Product Number
5
Dosage Form
-
Strength
5,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1992-07-20
Active Ingredient
HEPARIN SODIUM
Application Number
19802
Product Number
5
Dosage Form
-
Strength
5,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1992-07-20
Regulatory Status
Discontinued
Drug Name
HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5,000 UNITS/100ML
Approval Date
1985-03-29
Active Ingredient
HEPARIN SODIUM
Application Number
19135
Product Number
1
Dosage Form
-
Strength
5,000 UNITS/100ML
Approval Date
1985-03-29
Regulatory Status
Discontinued
Drug Name
HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
5,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1992-07-20
Active Ingredient
HEPARIN SODIUM
Application Number
19802
Product Number
3
Dosage Form
-
Strength
5,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1992-07-20
Regulatory Status
Discontinued
Drug Name
HEPARIN SODIUM 5,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
1,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-03-29
Active Ingredient
HEPARIN SODIUM
Application Number
19042
Product Number
4
Dosage Form
-
Strength
1,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-03-29
Regulatory Status
Discontinued
Drug Name
HEPATAMINE 8%
Product Number
1
Dosage Form
-
Strength
8% (8GM/100ML)
Approval Date
1982-08-03
Active Ingredient
AMINO ACIDS
Application Number
18676
Product Number
1
Dosage Form
-
Strength
8% (8GM/100ML)
Approval Date
1982-08-03
Regulatory Status
Discontinued
Drug Name
HYPROTIGEN 5%
Product Number
3
Dosage Form
-
Strength
5%
Approval Date
1984-01-10
Active Ingredient
PROTEIN HYDROLYSATE
Application Number
6170
Product Number
3
Dosage Form
-
Strength
5%
Approval Date
1984-01-10
Regulatory Status
Discontinued
Drug Name
ISOLYTE E IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
35MG/100ML;5GM/100ML;30MG/100ML;74MG/100ML;640MG/100ML;500MG/100ML;74MG/100ML
Approval Date
1993-12-20
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM CITRATE
Application Number
19867
Product Number
1
Dosage Form
-
Strength
35MG/100ML;5GM/100ML;30MG/100ML;74MG/100ML;640MG/100ML;500MG/100ML;74MG/100ML
Approval Date
1993-12-20
Regulatory Status
Discontinued
Drug Name
ISOLYTE E IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
35MG/100ML;30MG/100ML;74MG/100ML;640MG/100ML;500MG/100ML;74MG/100ML
Approval Date
1983-10-31
Active Ingredient
CALCIUM CHLORIDE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM CITRATE
Application Number
18899
Product Number
1
Dosage Form
-
Strength
35MG/100ML;30MG/100ML;74MG/100ML;640MG/100ML;500MG/100ML;74MG/100ML
Approval Date
1983-10-31
Regulatory Status
Discontinued
Drug Name
ISOLYTE E IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
35MG/100ML;30MG/100ML;74MG/100ML;640MG/100ML;500MG/100ML;74MG/100ML
Approval Date
1989-09-29
Active Ingredient
CALCIUM CHLORIDE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM CITRATE
Application Number
19718
Product Number
1
Dosage Form
-
Strength
35MG/100ML;30MG/100ML;74MG/100ML;640MG/100ML;500MG/100ML;74MG/100ML
Approval Date
1989-09-29
Regulatory Status
Discontinued
Drug Name
ISOLYTE E W/ DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
35MG/100ML;5GM/100ML;30MG/100ML;74MG/100ML;640MG/100ML;500MG/100ML;74MG/100ML
Approval Date
1983-01-17
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM CITRATE
Application Number
18269
Product Number
2
Dosage Form
-
Strength
35MG/100ML;5GM/100ML;30MG/100ML;74MG/100ML;640MG/100ML;500MG/100ML;74MG/100ML
Approval Date
1983-01-17
Regulatory Status
Discontinued
Drug Name
ISOLYTE H IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5GM/100ML;30MG/100ML;97MG/100ML;220MG/100ML;140MG/100ML
Approval Date
1993-06-10
Active Ingredient
DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
19844
Product Number
1
Dosage Form
-
Strength
5GM/100ML;30MG/100ML;97MG/100ML;220MG/100ML;140MG/100ML
Approval Date
1993-06-10
Regulatory Status
Discontinued
Drug Name
ISOLYTE H W/ DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5GM/100ML;30MG/100ML;97MG/100ML;220MG/100ML;140MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
18273
Product Number
1
Dosage Form
-
Strength
5GM/100ML;30MG/100ML;97MG/100ML;220MG/100ML;140MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ISOLYTE M IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5GM/100ML;150MG/100ML;130MG/100ML;280MG/100ML;91MG/100ML
Approval Date
1993-06-10
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
19870
Product Number
1
Dosage Form
-
Strength
5GM/100ML;150MG/100ML;130MG/100ML;280MG/100ML;91MG/100ML
Approval Date
1993-06-10
Regulatory Status
Discontinued
Drug Name
ISOLYTE M W/ DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5GM/100ML;150MG/100ML;130MG/100ML;280MG/100ML;91MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
18270
Product Number
1
Dosage Form
-
Strength
5GM/100ML;150MG/100ML;130MG/100ML;280MG/100ML;91MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ISOLYTE P W/ DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5GM/100ML;31MG/100ML;130MG/100ML;26MG/100ML;320MG/100ML
Approval Date
1984-12-27
Active Ingredient
DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM ACETATE
Application Number
19025
Product Number
1
Dosage Form
-
Strength
5GM/100ML;31MG/100ML;130MG/100ML;26MG/100ML;320MG/100ML
Approval Date
1984-12-27
Regulatory Status
Discontinued
Drug Name
ISOLYTE R IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
37MG/100ML;5GM/100ML;31MG/100ML;120MG/100ML;330MG/100ML;88MG/100ML
Approval Date
1993-06-10
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
19864
Product Number
1
Dosage Form
-
Strength
37MG/100ML;5GM/100ML;31MG/100ML;120MG/100ML;330MG/100ML;88MG/100ML
Approval Date
1993-06-10
Regulatory Status
Discontinued
Drug Name
ISOLYTE R W/ DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
37MG/100ML;5GM/100ML;31MG/100ML;120MG/100ML;330MG/100ML;88MG/100ML
Approval Date
1982-01-01
Active Ingredient
CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
18271
Product Number
1
Dosage Form
-
Strength
37MG/100ML;5GM/100ML;31MG/100ML;120MG/100ML;330MG/100ML;88MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ISOLYTE S IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5GM/100ML;30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML
Approval Date
1993-08-09
Active Ingredient
DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE
Application Number
19843
Product Number
1
Dosage Form
-
Strength
5GM/100ML;30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML
Approval Date
1993-08-09
Regulatory Status
Discontinued
Drug Name
ISOLYTE S IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML
Approval Date
1982-01-01
Active Ingredient
MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE
Application Number
18252
Product Number
1
Dosage Form
-
Strength
30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
ISOLYTE S PH 7.4 IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
30MG/100ML;37MG/100ML;0.82MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML;12MG/100ML
Approval Date
1984-04-04
Active Ingredient
MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Application Number
19006
Product Number
1
Dosage Form
-
Strength
30MG/100ML;37MG/100ML;0.82MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML;12MG/100ML
Approval Date
1984-04-04
Regulatory Status
Discontinued
Drug Name
ISOLYTE S W/ DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5GM/100ML;30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML
Approval Date
1982-01-01
Active Ingredient
DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE
Application Number
18274
Product Number
1
Dosage Form
-
Strength
5GM/100ML;30MG/100ML;37MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML
Approval Date
1982-01-01
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
1982-01-01
Active Ingredient
CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Application Number
18023
Product Number
1
Dosage Form
-
Strength
20MG/100ML;30MG/100ML;600MG/100ML;310MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
LIDOCAINE HYDROCHLORIDE 0.2% AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
200MG/100ML
Approval Date
1984-03-30
Active Ingredient
LIDOCAINE HYDROCHLORIDE
Application Number
18967
Product Number
1
Dosage Form
-
Strength
200MG/100ML
Approval Date
1984-03-30
Regulatory Status
Discontinued
Drug Name
LIDOCAINE HYDROCHLORIDE 0.4% AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
400MG/100ML
Approval Date
1984-03-30
Active Ingredient
LIDOCAINE HYDROCHLORIDE
Application Number
18967
Product Number
2
Dosage Form
-
Strength
400MG/100ML
Approval Date
1984-03-30
Regulatory Status
Discontinued
Drug Name
LIDOCAINE HYDROCHLORIDE 0.8% AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
800MG/100ML
Approval Date
1984-03-30
Active Ingredient
LIDOCAINE HYDROCHLORIDE
Application Number
18967
Product Number
3
Dosage Form
-
Strength
800MG/100ML
Approval Date
1984-03-30
Regulatory Status
Discontinued
Drug Name
MANNITOL 10%
Product Number
2
Dosage Form
-
Strength
10GM/100ML
Approval Date
1982-01-01
Active Ingredient
MANNITOL
Application Number
16080
Product Number
2
Dosage Form
-
Strength
10GM/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MANNITOL 10% W/ DEXTROSE 5% IN DISTILLED WATER
Product Number
6
Dosage Form
-
Strength
10GM/100ML
Approval Date
1982-01-01
Active Ingredient
MANNITOL
Application Number
16080
Product Number
6
Dosage Form
-
Strength
10GM/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MANNITOL 15%
Product Number
3
Dosage Form
-
Strength
15GM/100ML
Approval Date
1982-01-01
Active Ingredient
MANNITOL
Application Number
16080
Product Number
3
Dosage Form
-
Strength
15GM/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MANNITOL 15% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.45%
Product Number
5
Dosage Form
-
Strength
15GM/100ML
Approval Date
1982-01-01
Active Ingredient
MANNITOL
Application Number
16080
Product Number
5
Dosage Form
-
Strength
15GM/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MANNITOL 20%
Product Number
1
Dosage Form
-
Strength
20GM/100ML
Approval Date
1982-01-01
Active Ingredient
MANNITOL
Application Number
14738
Product Number
1
Dosage Form
-
Strength
20GM/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MANNITOL 20%
Product Number
4
Dosage Form
-
Strength
20GM/100ML
Approval Date
1982-01-01
Active Ingredient
MANNITOL
Application Number
16080
Product Number
4
Dosage Form
-
Strength
20GM/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MANNITOL 5%
Product Number
1
Dosage Form
-
Strength
5GM/100ML
Approval Date
1982-01-01
Active Ingredient
MANNITOL
Application Number
16080
Product Number
1
Dosage Form
-
Strength
5GM/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MANNITOL 5% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.12%
Product Number
7
Dosage Form
-
Strength
5GM/100ML
Approval Date
1982-01-01
Active Ingredient
MANNITOL
Application Number
16080
Product Number
7
Dosage Form
-
Strength
5GM/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
METRO I.V.
Product Number
1
Dosage Form
-
Strength
500MG/100ML
Approval Date
1982-08-31
Active Ingredient
METRONIDAZOLE
Application Number
18674
Product Number
1
Dosage Form
-
Strength
500MG/100ML
Approval Date
1982-08-31
Regulatory Status
Discontinued
Drug Name
METRO I.V. IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
500MG/100ML
Approval Date
1983-09-29
Active Ingredient
METRONIDAZOLE
Application Number
18900
Product Number
1
Dosage Form
-
Strength
500MG/100ML
Approval Date
1983-09-29
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
2004-08-18
Active Ingredient
MILRINONE LACTATE
Application Number
76414
Product Number
1
Dosage Form
-
Strength
EQ 20MG BASE/100ML (EQ 0.2MG BASE/ML)
Approval Date
2004-08-18
Regulatory Status
Discontinued
Drug Name
NEPHRAMINE 5.4%
Product Number
1
Dosage Form
-
Strength
5.4% (5.4GM/100ML)
Approval Date
1982-01-01
Active Ingredient
AMINO ACIDS
Application Number
17766
Product Number
1
Dosage Form
-
Strength
5.4% (5.4GM/100ML)
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
NUTRILIPID 10%
Product Number
1
Dosage Form
-
Strength
10%
Approval Date
1993-05-28
Active Ingredient
SOYBEAN OIL
Application Number
19531
Product Number
1
Dosage Form
-
Strength
10%
Approval Date
1993-05-28
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE 0.037% IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5GM/100ML;37MG/100ML
Approval Date
1989-09-29
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE
Application Number
19699
Product Number
1
Dosage Form
-
Strength
5GM/100ML;37MG/100ML
Approval Date
1989-09-29
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE 0.037% IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
37MG/100ML;900MG/100ML
Approval Date
1989-09-29
Active Ingredient
POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
19708
Product Number
1
Dosage Form
-
Strength
37MG/100ML;900MG/100ML
Approval Date
1989-09-29
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE 0.075% IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
5GM/100ML;75MG/100ML
Approval Date
1982-11-09
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE
Application Number
18744
Product Number
1
Dosage Form
-
Strength
5GM/100ML;75MG/100ML
Approval Date
1982-11-09
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE 0.075% IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
5GM/100ML;75MG/100ML
Approval Date
1989-09-29
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE
Application Number
19699
Product Number
2
Dosage Form
-
Strength
5GM/100ML;75MG/100ML
Approval Date
1989-09-29
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE 0.075% IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
75MG/100ML;900MG/100ML
Approval Date
1989-09-29
Active Ingredient
POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
19708
Product Number
2
Dosage Form
-
Strength
75MG/100ML;900MG/100ML
Approval Date
1989-09-29
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE 0.11% IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
5GM/100ML;110MG/100ML
Approval Date
1989-09-29
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE
Application Number
19699
Product Number
3
Dosage Form
-
Strength
5GM/100ML;110MG/100ML
Approval Date
1989-09-29
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE 0.11% IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
110MG/100ML;900MG/100ML
Approval Date
1989-09-29
Active Ingredient
POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
19708
Product Number
3
Dosage Form
-
Strength
110MG/100ML;900MG/100ML
Approval Date
1989-09-29
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
5GM/100ML;150MG/100ML
Approval Date
1982-11-09
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE
Application Number
18744
Product Number
2
Dosage Form
-
Strength
5GM/100ML;150MG/100ML
Approval Date
1982-11-09
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
5GM/100ML;220MG/100ML
Approval Date
1982-11-09
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE
Application Number
18744
Product Number
3
Dosage Form
-
Strength
5GM/100ML;220MG/100ML
Approval Date
1982-11-09
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE 0.22% IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
5
Dosage Form
-
Strength
5GM/100ML;220MG/100ML
Approval Date
1989-09-29
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE
Application Number
19699
Product Number
5
Dosage Form
-
Strength
5GM/100ML;220MG/100ML
Approval Date
1989-09-29
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE 0.22% IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
5
Dosage Form
-
Strength
220MG/100ML;900MG/100ML
Approval Date
1989-09-29
Active Ingredient
POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
19708
Product Number
5
Dosage Form
-
Strength
220MG/100ML;900MG/100ML
Approval Date
1989-09-29
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE 0.3% IN DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
5GM/100ML;300MG/100ML
Approval Date
1982-11-09
Active Ingredient
DEXTROSE; POTASSIUM CHLORIDE
Application Number
18744
Product Number
4
Dosage Form
-
Strength
5GM/100ML;300MG/100ML
Approval Date
1982-11-09
Regulatory Status
Discontinued
Drug Name
POTASSIUM CHLORIDE 0.3% IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Product Number
6
Dosage Form
-
Strength
300MG/100ML;900MG/100ML
Approval Date
1989-09-29
Active Ingredient
POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
19708
Product Number
6
Dosage Form
-
Strength
300MG/100ML;900MG/100ML
Approval Date
1989-09-29
Regulatory Status
Discontinued
Drug Name
PROCALAMINE
Product Number
1
Dosage Form
-
Strength
3%;26MG/100ML;3GM/100ML;54MG/100ML;41MG/100ML;150MG/100ML;200MG/100ML;120MG/100ML
Approval Date
1982-05-08
Active Ingredient
AMINO ACIDS; CALCIUM ACETATE; GLYCERIN; MAGNESIUM ACETATE; PHOSPHORIC ACID; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
Application Number
18582
Product Number
1
Dosage Form
-
Strength
3%;26MG/100ML;3GM/100ML;54MG/100ML;41MG/100ML;150MG/100ML;200MG/100ML;120MG/100ML
Approval Date
1982-05-08
Regulatory Status
Discontinued
Drug Name
RESECTISOL
Product Number
2
Dosage Form
-
Strength
5GM/100ML
Approval Date
1982-01-01
Active Ingredient
MANNITOL
Application Number
16704
Product Number
2
Dosage Form
-
Strength
5GM/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
RESECTISOL IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
5GM/100ML
Approval Date
1982-01-01
Active Ingredient
MANNITOL
Application Number
16772
Product Number
2
Dosage Form
-
Strength
5GM/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
RINGERS IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
33MG/100ML;30MG/100ML;860MG/100ML
Approval Date
1982-11-09
Active Ingredient
CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18721
Product Number
1
Dosage Form
-
Strength
33MG/100ML;30MG/100ML;860MG/100ML
Approval Date
1982-11-09
Regulatory Status
Discontinued
Drug Name
SODIUM CHLORIDE
Product Number
1
Dosage Form
-
Strength
20GM/100ML
Approval Date
1982-01-01
Active Ingredient
SODIUM CHLORIDE
Application Number
17038
Product Number
1
Dosage Form
-
Strength
20GM/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
1982-01-01
Active Ingredient
SODIUM CHLORIDE
Application Number
18184
Product Number
1
Dosage Form
-
Strength
450MG/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
75MG/100ML;900MG/100ML
Approval Date
1982-11-09
Active Ingredient
POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18722
Product Number
1
Dosage Form
-
Strength
75MG/100ML;900MG/100ML
Approval Date
1982-11-09
Regulatory Status
Discontinued
Drug Name
SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.15% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
150MG/100ML;900MG/100ML
Approval Date
1982-11-09
Active Ingredient
POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18722
Product Number
2
Dosage Form
-
Strength
150MG/100ML;900MG/100ML
Approval Date
1982-11-09
Regulatory Status
Discontinued
Drug Name
SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.22% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
220MG/100ML;900MG/100ML
Approval Date
1982-11-09
Active Ingredient
POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18722
Product Number
3
Dosage Form
-
Strength
220MG/100ML;900MG/100ML
Approval Date
1982-11-09
Regulatory Status
Discontinued
Drug Name
SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.3% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
300MG/100ML;900MG/100ML
Approval Date
1982-11-09
Active Ingredient
POTASSIUM CHLORIDE; SODIUM CHLORIDE
Application Number
18722
Product Number
4
Dosage Form
-
Strength
300MG/100ML;900MG/100ML
Approval Date
1982-11-09
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
18186
Product Number
1
Dosage Form
-
Strength
1.87GM/100ML
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
SODIUM LACTATE 1/6 MOLAR IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
1.87GM/100ML
Approval Date
1992-04-21
Active Ingredient
SODIUM LACTATE
Application Number
20004
Product Number
1
Dosage Form
-
Strength
1.87GM/100ML
Approval Date
1992-04-21
Regulatory Status
Discontinued
Drug Name
STERILE WATER FOR INJECTION IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
100%
Approval Date
1984-03-02
Active Ingredient
STERILE WATER FOR INJECTION
Application Number
19077
Product Number
1
Dosage Form
-
Strength
100%
Approval Date
1984-03-02
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE 0.04% AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
40MG/100ML
Approval Date
1984-11-07
Active Ingredient
THEOPHYLLINE
Application Number
19083
Product Number
1
Dosage Form
-
Strength
40MG/100ML
Approval Date
1984-11-07
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE 0.04% AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
40MG/100ML
Approval Date
1992-08-14
Active Ingredient
THEOPHYLLINE
Application Number
19826
Product Number
1
Dosage Form
-
Strength
40MG/100ML
Approval Date
1992-08-14
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE 0.08% AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
80MG/100ML
Approval Date
1984-11-07
Active Ingredient
THEOPHYLLINE
Application Number
19083
Product Number
2
Dosage Form
-
Strength
80MG/100ML
Approval Date
1984-11-07
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE 0.08% AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
80MG/100ML
Approval Date
1992-08-14
Active Ingredient
THEOPHYLLINE
Application Number
19826
Product Number
2
Dosage Form
-
Strength
80MG/100ML
Approval Date
1992-08-14
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE 0.16% AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
160MG/100ML
Approval Date
1984-11-07
Active Ingredient
THEOPHYLLINE
Application Number
19083
Product Number
3
Dosage Form
-
Strength
160MG/100ML
Approval Date
1984-11-07
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE 0.16% AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
160MG/100ML
Approval Date
1992-08-14
Active Ingredient
THEOPHYLLINE
Application Number
19826
Product Number
3
Dosage Form
-
Strength
160MG/100ML
Approval Date
1992-08-14
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE 0.2% AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
200MG/100ML
Approval Date
1984-11-07
Active Ingredient
THEOPHYLLINE
Application Number
19212
Product Number
1
Dosage Form
-
Strength
200MG/100ML
Approval Date
1984-11-07
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE 0.2% AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
4
Dosage Form
-
Strength
200MG/100ML
Approval Date
1992-08-14
Active Ingredient
THEOPHYLLINE
Application Number
19826
Product Number
4
Dosage Form
-
Strength
200MG/100ML
Approval Date
1992-08-14
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE 0.32% AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
6
Dosage Form
-
Strength
320MG/100ML
Approval Date
1992-08-14
Active Ingredient
THEOPHYLLINE
Application Number
19826
Product Number
6
Dosage Form
-
Strength
320MG/100ML
Approval Date
1992-08-14
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE 0.4% AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
2
Dosage Form
-
Strength
400MG/100ML
Approval Date
1984-11-07
Active Ingredient
THEOPHYLLINE
Application Number
19212
Product Number
2
Dosage Form
-
Strength
400MG/100ML
Approval Date
1984-11-07
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE 0.4% AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
3
Dosage Form
-
Strength
4MG/ML
Approval Date
1984-11-07
Active Ingredient
THEOPHYLLINE
Application Number
19212
Product Number
3
Dosage Form
-
Strength
4MG/ML
Approval Date
1984-11-07
Regulatory Status
Discontinued
Drug Name
THEOPHYLLINE 0.4% AND DEXTROSE 5% IN PLASTIC CONTAINER
Product Number
5
Dosage Form
-
Strength
400MG/100ML
Approval Date
1992-08-14
Active Ingredient
THEOPHYLLINE
Application Number
19826
Product Number
5
Dosage Form
-
Strength
400MG/100ML
Approval Date
1992-08-14
Regulatory Status
Discontinued
Drug Name
UCEPHAN
Product Number
1
Dosage Form
-
Strength
100MG/ML;100MG/ML
Approval Date
1987-12-23
Active Ingredient
SODIUM BENZOATE; SODIUM PHENYLACETATE
Application Number
19530
Product Number
1
Dosage Form
-
Strength
100MG/ML;100MG/ML
Approval Date
1987-12-23
Regulatory Status
Discontinued
Drug Status Breakdown
167 total- Discontinued
Official Source
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Drug Name
ACETATED RINGERS IN PLASTIC CONTAINER
Application Number
18725
Product Number
1
Active Ingredient
CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE
Dosage Form
-
Strength
20MG/100ML;30MG/100ML;380MG/100ML;600MG/100ML
FDA Approved Drug Data
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