Wyeth Pharmaceuticals Inc Discontinued
FDA Approved Drugs
Wyeth Pharmaceuticals Inc 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 52
- Latest Approval Date May 22, 2007
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Overview
Social Profiles
Company Snapshot
Wyeth Pharmaceuticals Inc Discontinued
500 Arcola Road Collegeville, PA 19426
U.S.A
www.wyeth.com View on MapFDA Approved Drug Records ( 52 records )
Drug Name
CORDARONE
Product Number
1
Dosage Form
-
Strength
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-12-24
Active Ingredient
AMIODARONE HYDROCHLORIDE
Application Number
18972
Product Number
1
Dosage Form
-
Strength
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-12-24
Regulatory Status
Discontinued
Drug Name
CORDARONE
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50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
1995-08-03
Active Ingredient
AMIODARONE HYDROCHLORIDE
Application Number
20377
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50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
1995-08-03
Regulatory Status
Discontinued
Drug Name
EFFEXOR
Product Number
1
Dosage Form
-
Strength
EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-12-28
Active Ingredient
VENLAFAXINE HYDROCHLORIDE
Application Number
20151
Product Number
1
Dosage Form
-
Strength
EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-12-28
Regulatory Status
Discontinued
Drug Name
EFFEXOR
Product Number
2
Dosage Form
-
Strength
EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-12-28
Active Ingredient
VENLAFAXINE HYDROCHLORIDE
Application Number
20151
Product Number
2
Dosage Form
-
Strength
EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-12-28
Regulatory Status
Discontinued
Drug Name
EFFEXOR
Product Number
3
Dosage Form
-
Strength
EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-12-28
Active Ingredient
VENLAFAXINE HYDROCHLORIDE
Application Number
20151
Product Number
3
Dosage Form
-
Strength
EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-12-28
Regulatory Status
Discontinued
Drug Name
EFFEXOR
Product Number
4
Dosage Form
-
Strength
EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-12-28
Active Ingredient
VENLAFAXINE HYDROCHLORIDE
Application Number
20151
Product Number
4
Dosage Form
-
Strength
EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-12-28
Regulatory Status
Discontinued
Drug Name
EFFEXOR
Product Number
5
Dosage Form
-
Strength
EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-12-28
Active Ingredient
VENLAFAXINE HYDROCHLORIDE
Application Number
20151
Product Number
5
Dosage Form
-
Strength
EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-12-28
Regulatory Status
Discontinued
Drug Name
EFFEXOR
Product Number
6
Dosage Form
-
Strength
EQ 37.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-12-28
Active Ingredient
VENLAFAXINE HYDROCHLORIDE
Application Number
20151
Product Number
6
Dosage Form
-
Strength
EQ 37.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-12-28
Regulatory Status
Discontinued
Drug Name
FOLVITE
Product Number
4
Dosage Form
-
Strength
1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
FOLIC ACID
Application Number
5897
Product Number
4
Dosage Form
-
Strength
1MG **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
FOLVITE
Product Number
8
Dosage Form
-
Strength
5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
FOLIC ACID
Application Number
5897
Product Number
8
Dosage Form
-
Strength
5MG/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
INDERAL
Product Number
1
Dosage Form
-
Strength
10MG **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
16418
Product Number
1
Dosage Form
-
Strength
10MG **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
INDERAL
Product Number
2
Dosage Form
-
Strength
40MG **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
16418
Product Number
2
Dosage Form
-
Strength
40MG **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
INDERAL
Product Number
3
Dosage Form
-
Strength
20MG **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
16418
Product Number
3
Dosage Form
-
Strength
20MG **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
INDERAL
Product Number
4
Dosage Form
-
Strength
80MG **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
16418
Product Number
4
Dosage Form
-
Strength
80MG **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
INDERAL
Product Number
9
Dosage Form
-
Strength
60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-10-18
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
16418
Product Number
9
Dosage Form
-
Strength
60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-10-18
Regulatory Status
Discontinued
Drug Name
INDERAL
Product Number
10
Dosage Form
-
Strength
90MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-10-18
Active Ingredient
PROPRANOLOL HYDROCHLORIDE
Application Number
16418
Product Number
10
Dosage Form
-
Strength
90MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-10-18
Regulatory Status
Discontinued
Drug Name
INDERIDE-40/25
Product Number
1
Dosage Form
-
Strength
25MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
Application Number
18031
Product Number
1
Dosage Form
-
Strength
25MG;40MG **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
INDERIDE-80/25
Product Number
2
Dosage Form
-
Strength
25MG;80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
Application Number
18031
Product Number
2
Dosage Form
-
Strength
25MG;80MG **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
LEVONORGESTREL
Product Number
1
Dosage Form
-
Strength
75MG/IMPLANT
Approval Date
1996-08-15
Active Ingredient
LEVONORGESTREL
Application Number
20627
Product Number
1
Dosage Form
-
Strength
75MG/IMPLANT
Approval Date
1996-08-15
Regulatory Status
Discontinued
Drug Name
LO/OVRAL-28
Product Number
1
Dosage Form
-
Strength
0.03MG;0.3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
ETHINYL ESTRADIOL; NORGESTREL
Application Number
17802
Product Number
1
Dosage Form
-
Strength
0.03MG;0.3MG **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
LODINE
Product Number
2
Dosage Form
-
Strength
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-01-31
Active Ingredient
ETODOLAC
Application Number
18922
Product Number
2
Dosage Form
-
Strength
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1991-01-31
Regulatory Status
Discontinued
Drug Name
LODINE
Product Number
3
Dosage Form
-
Strength
300MG
Approval Date
1991-01-31
Active Ingredient
ETODOLAC
Application Number
18922
Product Number
3
Dosage Form
-
Strength
300MG
Approval Date
1991-01-31
Regulatory Status
Discontinued
Drug Name
LODINE
Product Number
4
Dosage Form
-
Strength
400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-07-29
Active Ingredient
ETODOLAC
Application Number
18922
Product Number
4
Dosage Form
-
Strength
400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-07-29
Regulatory Status
Discontinued
Drug Name
LODINE
Product Number
5
Dosage Form
-
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1996-06-28
Active Ingredient
ETODOLAC
Application Number
18922
Product Number
5
Dosage Form
-
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1996-06-28
Regulatory Status
Discontinued
Drug Name
LODINE XL
Product Number
1
Dosage Form
-
Strength
400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1996-10-25
Active Ingredient
ETODOLAC
Application Number
20584
Product Number
1
Dosage Form
-
Strength
400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1996-10-25
Regulatory Status
Discontinued
Drug Name
LODINE XL
Product Number
2
Dosage Form
-
Strength
600MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1996-10-25
Active Ingredient
ETODOLAC
Application Number
20584
Product Number
2
Dosage Form
-
Strength
600MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1996-10-25
Regulatory Status
Discontinued
Drug Name
LODINE XL
Product Number
3
Dosage Form
-
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1998-01-20
Active Ingredient
ETODOLAC
Application Number
20584
Product Number
3
Dosage Form
-
Strength
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1998-01-20
Regulatory Status
Discontinued
Drug Name
LYBREL
Product Number
1
Dosage Form
-
Strength
0.02MG;0.09MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2007-05-22
Active Ingredient
ETHINYL ESTRADIOL; LEVONORGESTREL
Application Number
21864
Product Number
1
Dosage Form
-
Strength
0.02MG;0.09MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
2007-05-22
Regulatory Status
Discontinued
Drug Name
NORPLANT SYSTEM IN PLASTIC CONTAINER
Product Number
1
Dosage Form
-
Strength
36MG/IMPLANT
Approval Date
1990-12-10
Active Ingredient
LEVONORGESTREL
Application Number
20088
Product Number
1
Dosage Form
-
Strength
36MG/IMPLANT
Approval Date
1990-12-10
Regulatory Status
Discontinued
Drug Name
ORUVAIL
Product Number
1
Dosage Form
-
Strength
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-09-24
Active Ingredient
KETOPROFEN
Application Number
19816
Product Number
1
Dosage Form
-
Strength
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-09-24
Regulatory Status
Discontinued
Drug Name
ORUVAIL
Product Number
2
Dosage Form
-
Strength
150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-02-08
Active Ingredient
KETOPROFEN
Application Number
19816
Product Number
2
Dosage Form
-
Strength
150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-02-08
Regulatory Status
Discontinued
Drug Name
ORUVAIL
Product Number
3
Dosage Form
-
Strength
100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-02-08
Active Ingredient
KETOPROFEN
Application Number
19816
Product Number
3
Dosage Form
-
Strength
100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1995-02-08
Regulatory Status
Discontinued
Drug Name
OVRAL
Product Number
1
Dosage Form
-
Strength
0.05MG;0.5MG
Approval Date
1982-01-01
Active Ingredient
ETHINYL ESTRADIOL; NORGESTREL
Application Number
16672
Product Number
1
Dosage Form
-
Strength
0.05MG;0.5MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
OVRAL-28
Product Number
1
Dosage Form
-
Strength
0.05MG;0.5MG
Approval Date
1982-01-01
Active Ingredient
ETHINYL ESTRADIOL; NORGESTREL
Application Number
16806
Product Number
1
Dosage Form
-
Strength
0.05MG;0.5MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PIPRACIL
Product Number
2
Dosage Form
-
Strength
EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
PIPERACILLIN SODIUM
Application Number
50545
Product Number
2
Dosage Form
-
Strength
EQ 2GM BASE/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
PIPRACIL
Product Number
3
Dosage Form
-
Strength
EQ 3GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
PIPERACILLIN SODIUM
Application Number
50545
Product Number
3
Dosage Form
-
Strength
EQ 3GM BASE/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
PIPRACIL
Product Number
4
Dosage Form
-
Strength
EQ 4GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1982-01-01
Active Ingredient
PIPERACILLIN SODIUM
Application Number
50545
Product Number
4
Dosage Form
-
Strength
EQ 4GM BASE/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
PIPRACIL
Product Number
6
Dosage Form
-
Strength
EQ 40GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-09-30
Active Ingredient
PIPERACILLIN SODIUM
Application Number
50545
Product Number
6
Dosage Form
-
Strength
EQ 40GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1985-09-30
Regulatory Status
Discontinued
Drug Name
PIPRACIL
Product Number
1
Dosage Form
-
Strength
EQ 2GM BASE/VIAL
Approval Date
1987-10-13
Active Ingredient
PIPERACILLIN SODIUM
Application Number
62750
Product Number
1
Dosage Form
-
Strength
EQ 2GM BASE/VIAL
Approval Date
1987-10-13
Regulatory Status
Discontinued
Drug Name
PIPRACIL
Product Number
2
Dosage Form
-
Strength
EQ 3GM BASE/VIAL
Approval Date
1987-10-13
Active Ingredient
PIPERACILLIN SODIUM
Application Number
62750
Product Number
2
Dosage Form
-
Strength
EQ 3GM BASE/VIAL
Approval Date
1987-10-13
Regulatory Status
Discontinued
Drug Name
PIPRACIL
Product Number
3
Dosage Form
-
Strength
EQ 4GM BASE/VIAL
Approval Date
1987-10-13
Active Ingredient
PIPERACILLIN SODIUM
Application Number
62750
Product Number
3
Dosage Form
-
Strength
EQ 4GM BASE/VIAL
Approval Date
1987-10-13
Regulatory Status
Discontinued
Drug Name
PREMARIN
Product Number
2
Dosage Form
-
Strength
2.5MG
Approval Date
1982-01-01
Active Ingredient
ESTROGENS, CONJUGATED
Application Number
4782
Product Number
2
Dosage Form
-
Strength
2.5MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PREMPHASE (PREMARIN;CYCRIN 14/14)
Product Number
2
Dosage Form
-
Strength
0.625MG,0.625MG;N/A,5MG
Approval Date
1994-12-30
Active Ingredient
ESTROGENS, CONJUGATED; MEDROXYPROGESTERONE ACETATE
Application Number
20303
Product Number
2
Dosage Form
-
Strength
0.625MG,0.625MG;N/A,5MG
Approval Date
1994-12-30
Regulatory Status
Discontinued
Drug Name
PREMPRO (PREMARIN;CYCRIN)
Product Number
1
Dosage Form
-
Strength
0.625MG,0.625MG;2.5MG,2.5MG
Approval Date
1994-12-30
Active Ingredient
ESTROGENS, CONJUGATED; MEDROXYPROGESTERONE ACETATE
Application Number
20303
Product Number
1
Dosage Form
-
Strength
0.625MG,0.625MG;2.5MG,2.5MG
Approval Date
1994-12-30
Regulatory Status
Discontinued
Drug Name
QUINIDEX
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
1982-01-01
Active Ingredient
QUINIDINE SULFATE
Application Number
12796
Product Number
2
Dosage Form
-
Strength
300MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TRECATOR
Product Number
2
Dosage Form
-
Strength
250MG
Approval Date
1982-01-01
Active Ingredient
ETHIONAMIDE
Application Number
13026
Product Number
2
Dosage Form
-
Strength
250MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
TRIPHASIL-21
Product Number
1
Dosage Form
-
Strength
0.03MG,0.04MG,0.03MG;0.05MG,0.075MG,0.125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-11-01
Active Ingredient
ETHINYL ESTRADIOL; LEVONORGESTREL
Application Number
19192
Product Number
1
Dosage Form
-
Strength
0.03MG,0.04MG,0.03MG;0.05MG,0.075MG,0.125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-11-01
Regulatory Status
Discontinued
Drug Name
TRIPHASIL-28
Product Number
1
Dosage Form
-
Strength
0.03MG,0.04MG,0.03MG;0.05MG,0.075MG,0.125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-11-01
Active Ingredient
ETHINYL ESTRADIOL; LEVONORGESTREL
Application Number
19190
Product Number
1
Dosage Form
-
Strength
0.03MG,0.04MG,0.03MG;0.05MG,0.075MG,0.125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1984-11-01
Regulatory Status
Discontinued
Drug Name
ZOSYN
Product Number
1
Dosage Form
-
Strength
EQ 2GM BASE/VIAL;EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-10-22
Active Ingredient
PIPERACILLIN SODIUM; TAZOBACTAM SODIUM
Application Number
50684
Product Number
1
Dosage Form
-
Strength
EQ 2GM BASE/VIAL;EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-10-22
Regulatory Status
Discontinued
Drug Name
ZOSYN
Product Number
2
Dosage Form
-
Strength
EQ 3GM BASE/VIAL;EQ 375MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-10-22
Active Ingredient
PIPERACILLIN SODIUM; TAZOBACTAM SODIUM
Application Number
50684
Product Number
2
Dosage Form
-
Strength
EQ 3GM BASE/VIAL;EQ 375MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-10-22
Regulatory Status
Discontinued
Drug Name
ZOSYN
Product Number
3
Dosage Form
-
Strength
EQ 4GM BASE/VIAL;EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-10-22
Active Ingredient
PIPERACILLIN SODIUM; TAZOBACTAM SODIUM
Application Number
50684
Product Number
3
Dosage Form
-
Strength
EQ 4GM BASE/VIAL;EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-10-22
Regulatory Status
Discontinued
Drug Name
ZOSYN
Product Number
4
Dosage Form
-
Strength
EQ 36GM BASE/VIAL;EQ 4.5GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-10-22
Active Ingredient
PIPERACILLIN SODIUM; TAZOBACTAM SODIUM
Application Number
50684
Product Number
4
Dosage Form
-
Strength
EQ 36GM BASE/VIAL;EQ 4.5GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date
1993-10-22
Regulatory Status
Discontinued
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Drug Status Breakdown
52 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
CORDARONE
Application Number
18972
Product Number
1
Active Ingredient
AMIODARONE HYDROCHLORIDE
Dosage Form
-
Strength
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
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