West-ward Pharmaceutical Corp Discontinued
FDA Approved Drugs
West-ward Pharmaceutical Corp 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 43
- Latest Approval Date Oct 26, 2011
- Data Source FDA
- First Approval Date Jan 01, 1982
Company Overview
Company
West-ward Pharmaceutical Corp Discontinued
Country
U.S.A
Website
Social Profiles
Company Snapshot
West-ward Pharmaceutical Corp Discontinued
401 Industrial Way WestEatontown, NJ 07724
U.S.A
www.west-ward.com/ International@west-ward.net, API@west-ward.net View on MapFDA Approved Drug Records ( 43 records )
Drug Name
ACETAMINOPHEN, CAFFEINE, AND DIHYDROCODEINE BITARTRATE
Product Number
1
Dosage Form
-
Strength
712.8MG;60MG;32MG
Approval Date
2006-09-22
Active Ingredient
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Application Number
40637
Product Number
1
Dosage Form
-
Strength
712.8MG;60MG;32MG
Approval Date
2006-09-22
Regulatory Status
Discontinued
Drug Name
AMITRIPTYLINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
AMITRIPTYLINE HYDROCHLORIDE
Application Number
87278
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
AMITRIPTYLINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-03-05
Active Ingredient
AMITRIPTYLINE HYDROCHLORIDE
Application Number
87647
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-03-05
Regulatory Status
Discontinued
Drug Name
CEFOTETAN
Product Number
1
Dosage Form
-
Strength
EQ 10GM BASE/VIAL
Approval Date
2011-10-26
Active Ingredient
CEFOTETAN DISODIUM
Application Number
91030
Product Number
1
Dosage Form
-
Strength
EQ 10GM BASE/VIAL
Approval Date
2011-10-26
Regulatory Status
Discontinued
Drug Name
CHLORDIAZEPOXIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Active Ingredient
CHLORDIAZEPOXIDE HYDROCHLORIDE
Application Number
85000
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CHLORDIAZEPOXIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Active Ingredient
CHLORDIAZEPOXIDE HYDROCHLORIDE
Application Number
85014
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CHLORDIAZEPOXIDE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
CHLORDIAZEPOXIDE HYDROCHLORIDE
Application Number
85294
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CHLORPHENIRAMINE MALEATE
Product Number
1
Dosage Form
-
Strength
4MG
Approval Date
1982-01-01
Active Ingredient
CHLORPHENIRAMINE MALEATE
Application Number
83787
Product Number
1
Dosage Form
-
Strength
4MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
CHLORPROMAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-09-16
Active Ingredient
CHLORPROMAZINE HYDROCHLORIDE
Application Number
87783
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-09-16
Regulatory Status
Discontinued
Drug Name
CHLORPROMAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-09-16
Active Ingredient
CHLORPROMAZINE HYDROCHLORIDE
Application Number
87865
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-09-16
Regulatory Status
Discontinued
Drug Name
CHLORPROMAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1982-09-15
Active Ingredient
CHLORPROMAZINE HYDROCHLORIDE
Application Number
87878
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1982-09-15
Regulatory Status
Discontinued
Drug Name
CHLORPROMAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1982-09-16
Active Ingredient
CHLORPROMAZINE HYDROCHLORIDE
Application Number
87880
Product Number
1
Dosage Form
-
Strength
200MG
Approval Date
1982-09-16
Regulatory Status
Discontinued
Drug Name
CHLORPROMAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1982-09-15
Active Ingredient
CHLORPROMAZINE HYDROCHLORIDE
Application Number
87884
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1982-09-15
Regulatory Status
Discontinued
Drug Name
CYANOCOBALAMIN
Product Number
1
Dosage Form
-
Strength
1MG
Approval Date
1982-01-01
Active Ingredient
CYANOCOBALAMIN
Application Number
84264
Product Number
1
Dosage Form
-
Strength
1MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
HYDRALAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1983-05-27
Active Ingredient
HYDRALAZINE HYDROCHLORIDE
Application Number
88240
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1983-05-27
Regulatory Status
Discontinued
Drug Name
HYDRALAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1983-05-27
Active Ingredient
HYDRALAZINE HYDROCHLORIDE
Application Number
88241
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1983-05-27
Regulatory Status
Discontinued
Drug Name
HYDROCHLOROTHIAZIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
HYDROCHLOROTHIAZIDE
Application Number
84899
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
IMIPRAMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1983-05-26
Active Ingredient
IMIPRAMINE HYDROCHLORIDE
Application Number
88222
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1983-05-26
Regulatory Status
Discontinued
Drug Name
IMIPRAMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1983-05-26
Active Ingredient
IMIPRAMINE HYDROCHLORIDE
Application Number
88223
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1983-05-26
Regulatory Status
Discontinued
Drug Name
MEPROBAMATE
Product Number
2
Dosage Form
-
Strength
400MG
Approval Date
1982-01-01
Active Ingredient
MEPROBAMATE
Application Number
15417
Product Number
2
Dosage Form
-
Strength
400MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
MEPROBAMATE
Product Number
3
Dosage Form
-
Strength
200MG
Approval Date
1982-01-01
Active Ingredient
MEPROBAMATE
Application Number
15417
Product Number
3
Dosage Form
-
Strength
200MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
METHYLTESTOSTERONE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Active Ingredient
METHYLTESTOSTERONE
Application Number
84331
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
METHYLTESTOSTERONE
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
METHYLTESTOSTERONE
Application Number
84331
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
METHYLTESTOSTERONE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Active Ingredient
METHYLTESTOSTERONE
Application Number
84642
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PREDNISOLONE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Active Ingredient
PREDNISOLONE
Application Number
80324
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
PROPOXYPHENE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
65MG
Approval Date
1982-01-01
Active Ingredient
PROPOXYPHENE HYDROCHLORIDE
Application Number
83501
Product Number
1
Dosage Form
-
Strength
65MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
RESERPINE AND HYDROCHLOROTHIAZIDE-50
Product Number
1
Dosage Form
-
Strength
50MG;0.125MG
Approval Date
1984-05-10
Active Ingredient
HYDROCHLOROTHIAZIDE; RESERPINE
Application Number
88189
Product Number
1
Dosage Form
-
Strength
50MG;0.125MG
Approval Date
1984-05-10
Regulatory Status
Discontinued
Drug Name
RISPERIDONE
Product Number
1
Dosage Form
-
Strength
0.25MG
Approval Date
2009-05-29
Active Ingredient
RISPERIDONE
Application Number
78740
Product Number
1
Dosage Form
-
Strength
0.25MG
Approval Date
2009-05-29
Regulatory Status
Discontinued
Drug Name
RISPERIDONE
Product Number
2
Dosage Form
-
Strength
0.5MG
Approval Date
2009-05-29
Active Ingredient
RISPERIDONE
Application Number
78740
Product Number
2
Dosage Form
-
Strength
0.5MG
Approval Date
2009-05-29
Regulatory Status
Discontinued
Drug Name
RISPERIDONE
Product Number
3
Dosage Form
-
Strength
1MG
Approval Date
2009-05-29
Active Ingredient
RISPERIDONE
Application Number
78740
Product Number
3
Dosage Form
-
Strength
1MG
Approval Date
2009-05-29
Regulatory Status
Discontinued
Drug Name
RISPERIDONE
Product Number
4
Dosage Form
-
Strength
2MG
Approval Date
2009-05-29
Active Ingredient
RISPERIDONE
Application Number
78740
Product Number
4
Dosage Form
-
Strength
2MG
Approval Date
2009-05-29
Regulatory Status
Discontinued
Drug Name
RISPERIDONE
Product Number
5
Dosage Form
-
Strength
3MG
Approval Date
2009-05-29
Active Ingredient
RISPERIDONE
Application Number
78740
Product Number
5
Dosage Form
-
Strength
3MG
Approval Date
2009-05-29
Regulatory Status
Discontinued
Drug Name
RISPERIDONE
Product Number
6
Dosage Form
-
Strength
4MG
Approval Date
2009-05-29
Active Ingredient
RISPERIDONE
Application Number
78740
Product Number
6
Dosage Form
-
Strength
4MG
Approval Date
2009-05-29
Regulatory Status
Discontinued
Drug Name
SECOBARBITAL SODIUM
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1982-01-01
Active Ingredient
SECOBARBITAL SODIUM
Application Number
84926
Product Number
1
Dosage Form
-
Strength
100MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
SULFISOXAZOLE
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Active Ingredient
SULFISOXAZOLE
Application Number
80379
Product Number
1
Dosage Form
-
Strength
500MG
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
THIORIDAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1984-03-26
Active Ingredient
THIORIDAZINE HYDROCHLORIDE
Application Number
88658
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
1984-03-26
Regulatory Status
Discontinued
Drug Name
THIORIDAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
15MG
Approval Date
1984-03-26
Active Ingredient
THIORIDAZINE HYDROCHLORIDE
Application Number
88659
Product Number
1
Dosage Form
-
Strength
15MG
Approval Date
1984-03-26
Regulatory Status
Discontinued
Drug Name
THIORIDAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1984-03-26
Active Ingredient
THIORIDAZINE HYDROCHLORIDE
Application Number
88660
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
1984-03-26
Regulatory Status
Discontinued
Drug Name
THIORIDAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1984-03-26
Active Ingredient
THIORIDAZINE HYDROCHLORIDE
Application Number
88661
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
1984-03-26
Regulatory Status
Discontinued
Drug Name
TRIPROLIDINE AND PSEUDOEPHEDRINE
Product Number
1
Dosage Form
-
Strength
60MG;2.5MG
Approval Date
1983-04-19
Active Ingredient
PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE
Application Number
88117
Product Number
1
Dosage Form
-
Strength
60MG;2.5MG
Approval Date
1983-04-19
Regulatory Status
Discontinued
Drug Name
VITAMIN A
Product Number
1
Dosage Form
-
Strength
EQ 50,000 UNITS BASE
Approval Date
1982-01-01
Active Ingredient
VITAMIN A PALMITATE
Application Number
80967
Product Number
1
Dosage Form
-
Strength
EQ 50,000 UNITS BASE
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
VITAMIN A
Product Number
1
Dosage Form
-
Strength
50,000USP UNITS
Approval Date
1982-01-01
Active Ingredient
VITAMIN A
Application Number
80985
Product Number
1
Dosage Form
-
Strength
50,000USP UNITS
Approval Date
1982-01-01
Regulatory Status
Discontinued
Drug Name
VITAMIN D
Product Number
1
Dosage Form
-
Strength
50,000 IU
Approval Date
1982-01-01
Active Ingredient
ERGOCALCIFEROL
Application Number
83102
Product Number
1
Dosage Form
-
Strength
50,000 IU
Approval Date
1982-01-01
Regulatory Status
Discontinued
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Drug Status Breakdown
43 total- Discontinued
Official Source
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Drug Name
ACETAMINOPHEN, CAFFEINE, AND DIHYDROCODEINE BITARTRATE
Application Number
40637
Product Number
1
Active Ingredient
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE
Dosage Form
-
Strength
712.8MG;60MG;32MG
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