West-ward Pharmaceutical Corp
FDA Approved Drugs

West-ward Pharmaceutical Corp

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.

Discontinued RX
  • Total Records 46
  • Latest Approval Date Feb 28, 2017
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
46
View
Discontinued
43
View
RX
3
View
Company Overview

Company

West-ward Pharmaceutical Corp

Country

U.S.A

Website

Visit Website

Email

International@west-ward.net, API@west-ward.net

Social Profiles

Company Snapshot

West-ward Pharmaceutical Corp

401 Industrial Way WestEatontown, NJ 07724

U.S.A

www.west-ward.com/ International@west-ward.net, API@west-ward.net View on Map
FDA Approved Drug Records ( 46 records )
2006
22 Sep
Discontinued Application: 40637

Drug Name

ACETAMINOPHEN, CAFFEINE, AND DIHYDROCODEINE BITARTRATE

Product Number

1

Dosage Form

-

Strength

712.8MG;60MG;32MG

Approval Date

2006-09-22

40637 / 1

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

1982
01 Jan
Discontinued Application: 87278

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

87278 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

87278

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
05 Mar
Discontinued Application: 87647

Drug Name

AMITRIPTYLINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-03-05

87647 / 1

Active Ingredient

AMITRIPTYLINE HYDROCHLORIDE

Application Number

87647

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-03-05

Regulatory Status

Discontinued

2011
26 Oct
Discontinued Application: 91030

Drug Name

CEFOTETAN

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2011-10-26

91030 / 1

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

1982
01 Jan
Discontinued Application: 85000

Drug Name

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

85000 / 1

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

85000

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85014

Drug Name

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

85014 / 1

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

85014

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85294

Drug Name

CHLORDIAZEPOXIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

85294 / 1

Active Ingredient

CHLORDIAZEPOXIDE HYDROCHLORIDE

Application Number

85294

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83787

Drug Name

CHLORPHENIRAMINE MALEATE

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

83787 / 1

Active Ingredient

CHLORPHENIRAMINE MALEATE

Application Number

83787

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
16 Sep
Discontinued Application: 87783

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-09-16

87783 / 1

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

87783

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-09-16

Regulatory Status

Discontinued

1982
16 Sep
Discontinued Application: 87865

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-09-16

87865 / 1

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

87865

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-09-16

Regulatory Status

Discontinued

1982
15 Sep
Discontinued Application: 87878

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-09-15

87878 / 1

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

87878

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1982-09-15

Regulatory Status

Discontinued

1982
16 Sep
Discontinued Application: 87880

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-09-16

87880 / 1

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

87880

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-09-16

Regulatory Status

Discontinued

1982
15 Sep
Discontinued Application: 87884

Drug Name

CHLORPROMAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-09-15

87884 / 1

Active Ingredient

CHLORPROMAZINE HYDROCHLORIDE

Application Number

87884

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-09-15

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84264

Drug Name

CYANOCOBALAMIN

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

84264 / 1

Active Ingredient

CYANOCOBALAMIN

Application Number

84264

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1997
28 Feb
RX Application: 40204

Drug Name

DICYCLOMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1997-02-28

40204 / 1

Active Ingredient

DICYCLOMINE HYDROCHLORIDE

Application Number

40204

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1997-02-28

Regulatory Status

RX

1983
27 May
Discontinued Application: 88240

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-05-27

88240 / 1

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

88240

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-05-27

Regulatory Status

Discontinued

1983
27 May
Discontinued Application: 88241

Drug Name

HYDRALAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1983-05-27

88241 / 1

Active Ingredient

HYDRALAZINE HYDROCHLORIDE

Application Number

88241

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1983-05-27

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84899

Drug Name

HYDROCHLOROTHIAZIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

84899 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE

Application Number

84899

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1983
26 May
Discontinued Application: 88222

Drug Name

IMIPRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-05-26

88222 / 1

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

88222

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1983-05-26

Regulatory Status

Discontinued

1983
26 May
Discontinued Application: 88223

Drug Name

IMIPRAMINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1983-05-26

88223 / 1

Active Ingredient

IMIPRAMINE HYDROCHLORIDE

Application Number

88223

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1983-05-26

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 15417

Drug Name

MEPROBAMATE

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

15417 / 2

Active Ingredient

MEPROBAMATE

Application Number

15417

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 15417

Drug Name

MEPROBAMATE

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

15417 / 3

Active Ingredient

MEPROBAMATE

Application Number

15417

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84331

Drug Name

METHYLTESTOSTERONE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

84331 / 1

Active Ingredient

METHYLTESTOSTERONE

Application Number

84331

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84331

Drug Name

METHYLTESTOSTERONE

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

84331 / 2

Active Ingredient

METHYLTESTOSTERONE

Application Number

84331

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 84642

Drug Name

METHYLTESTOSTERONE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

84642 / 1

Active Ingredient

METHYLTESTOSTERONE

Application Number

84642

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80324

Drug Name

PREDNISOLONE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

80324 / 1

Active Ingredient

PREDNISOLONE

Application Number

80324

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83501

Drug Name

PROPOXYPHENE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

65MG

Approval Date

1982-01-01

83501 / 1

Active Ingredient

PROPOXYPHENE HYDROCHLORIDE

Application Number

83501

Product Number

1

Dosage Form

-

Strength

65MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984
10 May
Discontinued Application: 88189

Drug Name

RESERPINE AND HYDROCHLOROTHIAZIDE-50

Product Number

1

Dosage Form

-

Strength

50MG;0.125MG

Approval Date

1984-05-10

88189 / 1

Active Ingredient

HYDROCHLOROTHIAZIDE; RESERPINE

Application Number

88189

Product Number

1

Dosage Form

-

Strength

50MG;0.125MG

Approval Date

1984-05-10

Regulatory Status

Discontinued

2009
29 May
Discontinued Application: 78740

Drug Name

RISPERIDONE

Product Number

1

Dosage Form

-

Strength

0.25MG

Approval Date

2009-05-29

78740 / 1

Active Ingredient

RISPERIDONE

Application Number

78740

Product Number

1

Dosage Form

-

Strength

0.25MG

Approval Date

2009-05-29

Regulatory Status

Discontinued

2009
29 May
Discontinued Application: 78740

Drug Name

RISPERIDONE

Product Number

2

Dosage Form

-

Strength

0.5MG

Approval Date

2009-05-29

78740 / 2

Active Ingredient

RISPERIDONE

Application Number

78740

Product Number

2

Dosage Form

-

Strength

0.5MG

Approval Date

2009-05-29

Regulatory Status

Discontinued

2009
29 May
Discontinued Application: 78740

Drug Name

RISPERIDONE

Product Number

3

Dosage Form

-

Strength

1MG

Approval Date

2009-05-29

78740 / 3

Active Ingredient

RISPERIDONE

Application Number

78740

Product Number

3

Dosage Form

-

Strength

1MG

Approval Date

2009-05-29

Regulatory Status

Discontinued

2009
29 May
Discontinued Application: 78740

Drug Name

RISPERIDONE

Product Number

4

Dosage Form

-

Strength

2MG

Approval Date

2009-05-29

78740 / 4

Active Ingredient

RISPERIDONE

Application Number

78740

Product Number

4

Dosage Form

-

Strength

2MG

Approval Date

2009-05-29

Regulatory Status

Discontinued

2009
29 May
Discontinued Application: 78740

Drug Name

RISPERIDONE

Product Number

5

Dosage Form

-

Strength

3MG

Approval Date

2009-05-29

78740 / 5

Active Ingredient

RISPERIDONE

Application Number

78740

Product Number

5

Dosage Form

-

Strength

3MG

Approval Date

2009-05-29

Regulatory Status

Discontinued

2009
29 May
Discontinued Application: 78740

Drug Name

RISPERIDONE

Product Number

6

Dosage Form

-

Strength

4MG

Approval Date

2009-05-29

78740 / 6

Active Ingredient

RISPERIDONE

Application Number

78740

Product Number

6

Dosage Form

-

Strength

4MG

Approval Date

2009-05-29

Regulatory Status

Discontinued

2017
28 Feb
RX Application: 204679

Drug Name

ROCURONIUM BROMIDE

Product Number

1

Dosage Form

-

Strength

50MG/5ML (10MG/ML)

Approval Date

2017-02-28

204679 / 1

Active Ingredient

ROCURONIUM BROMIDE

Application Number

204679

Product Number

1

Dosage Form

-

Strength

50MG/5ML (10MG/ML)

Approval Date

2017-02-28

Regulatory Status

RX

2017
28 Feb
RX Application: 204679

Drug Name

ROCURONIUM BROMIDE

Product Number

2

Dosage Form

-

Strength

100MG/10ML (10MG/ML)

Approval Date

2017-02-28

204679 / 2

Active Ingredient

ROCURONIUM BROMIDE

Application Number

204679

Product Number

2

Dosage Form

-

Strength

100MG/10ML (10MG/ML)

Approval Date

2017-02-28

Regulatory Status

RX

1982
01 Jan
Discontinued Application: 84926

Drug Name

SECOBARBITAL SODIUM

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

84926 / 1

Active Ingredient

SECOBARBITAL SODIUM

Application Number

84926

Product Number

1

Dosage Form

-

Strength

100MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80379

Drug Name

SULFISOXAZOLE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

80379 / 1

Active Ingredient

SULFISOXAZOLE

Application Number

80379

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1984
26 Mar
Discontinued Application: 88658

Drug Name

THIORIDAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1984-03-26

88658 / 1

Active Ingredient

THIORIDAZINE HYDROCHLORIDE

Application Number

88658

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1984-03-26

Regulatory Status

Discontinued

1984
26 Mar
Discontinued Application: 88659

Drug Name

THIORIDAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1984-03-26

88659 / 1

Active Ingredient

THIORIDAZINE HYDROCHLORIDE

Application Number

88659

Product Number

1

Dosage Form

-

Strength

15MG

Approval Date

1984-03-26

Regulatory Status

Discontinued

1984
26 Mar
Discontinued Application: 88660

Drug Name

THIORIDAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1984-03-26

88660 / 1

Active Ingredient

THIORIDAZINE HYDROCHLORIDE

Application Number

88660

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

1984-03-26

Regulatory Status

Discontinued

1984
26 Mar
Discontinued Application: 88661

Drug Name

THIORIDAZINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1984-03-26

88661 / 1

Active Ingredient

THIORIDAZINE HYDROCHLORIDE

Application Number

88661

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1984-03-26

Regulatory Status

Discontinued

1983
19 Apr
Discontinued Application: 88117

Drug Name

TRIPROLIDINE AND PSEUDOEPHEDRINE

Product Number

1

Dosage Form

-

Strength

60MG;2.5MG

Approval Date

1983-04-19

88117 / 1

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

1982
01 Jan
Discontinued Application: 80967

Drug Name

VITAMIN A

Product Number

1

Dosage Form

-

Strength

EQ 50,000 UNITS BASE

Approval Date

1982-01-01

80967 / 1

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

1982
01 Jan
Discontinued Application: 80985

Drug Name

VITAMIN A

Product Number

1

Dosage Form

-

Strength

50,000USP UNITS

Approval Date

1982-01-01

80985 / 1

Active Ingredient

VITAMIN A

Application Number

80985

Product Number

1

Dosage Form

-

Strength

50,000USP UNITS

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83102

Drug Name

VITAMIN D

Product Number

1

Dosage Form

-

Strength

50,000 IU

Approval Date

1982-01-01

83102 / 1

Active Ingredient

ERGOCALCIFEROL

Application Number

83102

Product Number

1

Dosage Form

-

Strength

50,000 IU

Approval Date

1982-01-01

Regulatory Status

Discontinued

Related Databases
  • FDA Inspections
    0 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    46 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
46 total
  • Discontinued
  • RX
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

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

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.
Login to Submit