Contract Pharmacal Corporation Discontinued
FDA Approved Drugs

Contract Pharmacal Corporation Discontinued

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

Discontinued
  • Total Records 13
  • Latest Approval Date Apr 08, 2002
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
28
View
Unclassified
2
View
Discontinued
13
View
OTC
7
View
RX
6
View
Company Overview

Company

Contract Pharmacal Corporation Discontinued

Country

U.S.A

Website

Visit Website

Email

info@cpc.com

Social Profiles

LinkedIn
Company Snapshot

Contract Pharmacal Corporation Discontinued

165 Oser Avenue Hauppauge, NY 11788

U.S.A

www.cpc.com/ info@cpc.com View on Map
FDA Approved Drug Records ( 13 records )
1998
19 Jun
Discontinued Application: 74961

Drug Name

CIMETIDINE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1998-06-19

74961 / 1

Active Ingredient

CIMETIDINE

Application Number

74961

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1998-06-19

Regulatory Status

Discontinued

1998
19 Jun
Discontinued Application: 74963

Drug Name

CIMETIDINE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1998-06-19

74963 / 1

Active Ingredient

CIMETIDINE

Application Number

74963

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1998-06-19

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 85061

Drug Name

FOLIC ACID

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

85061 / 1

Active Ingredient

FOLIC ACID

Application Number

85061

Product Number

1

Dosage Form

-

Strength

1MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1987
10 Sep
Discontinued Application: 71735

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1987-09-10

71735 / 1

Active Ingredient

IBUPROFEN

Application Number

71735

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1987-09-10

Regulatory Status

Discontinued

1994
25 Feb
Discontinued Application: 73691

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1994-02-25

73691 / 1

Active Ingredient

IBUPROFEN

Application Number

73691

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1994-02-25

Regulatory Status

Discontinued

1998
06 Jul
Discontinued Application: 74782

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1998-07-06

74782 / 1

Active Ingredient

IBUPROFEN

Application Number

74782

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1998-07-06

Regulatory Status

Discontinued

1998
20 Jul
Discontinued Application: 74931

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1998-07-20

74931 / 1

Active Ingredient

IBUPROFEN

Application Number

74931

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1998-07-20

Regulatory Status

Discontinued

2002
08 Apr
Discontinued Application: 75588

Drug Name

IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

200MG;30MG

Approval Date

2002-04-08

75588 / 1

Active Ingredient

IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE

Application Number

75588

Product Number

1

Dosage Form

-

Strength

200MG;30MG

Approval Date

2002-04-08

Regulatory Status

Discontinued

1993
30 Jul
Discontinued Application: 73254

Drug Name

LOPERAMIDE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1993-07-30

73254 / 1

Active Ingredient

LOPERAMIDE HYDROCHLORIDE

Application Number

73254

Product Number

1

Dosage Form

-

Strength

2MG

Approval Date

1993-07-30

Regulatory Status

Discontinued

1997
27 Feb
Discontinued Application: 74789

Drug Name

NAPROXEN SODIUM

Product Number

1

Dosage Form

-

Strength

220MG

Approval Date

1997-02-27

74789 / 1

Active Ingredient

NAPROXEN SODIUM

Application Number

74789

Product Number

1

Dosage Form

-

Strength

220MG

Approval Date

1997-02-27

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 80209

Drug Name

PREDNISONE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

80209 / 1

Active Ingredient

PREDNISONE

Application Number

80209

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1982
01 Jan
Discontinued Application: 83808

Drug Name

QUINIDINE SULFATE

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

83808 / 1

Active Ingredient

QUINIDINE SULFATE

Application Number

83808

Product Number

1

Dosage Form

-

Strength

200MG

Approval Date

1982-01-01

Regulatory Status

Discontinued

1999
21 Jun
Discontinued Application: 75094

Drug Name

RANITIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

1999-06-21

75094 / 1

Active Ingredient

RANITIDINE HYDROCHLORIDE

Application Number

75094

Product Number

1

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

1999-06-21

Regulatory Status

Discontinued

Related Databases
  • FDA Inspections
    30 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    0 View
  • FDA Approved Drugs Database
    28 View
  • Drug Prices in Switzerland
    0 View
Drug Status Breakdown
13 total
  • Discontinued
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

CIMETIDINE

Application Number

74961

Product Number

1

Active Ingredient

CIMETIDINE

Dosage Form

-

Strength

200MG

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