Contract Pharmacal Corporation
FDA Approved Drugs

Contract Pharmacal Corporation

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.

OTC Discontinued RX Unclassified
  • Total Records 28
  • Latest Approval Date Mar 09, 2026
  • 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

Country

U.S.A

Website

Visit Website

Email

info@cpc.com

Social Profiles

LinkedIn
Company Snapshot

Contract Pharmacal Corporation

165 Oser Avenue Hauppauge, NY 11788

U.S.A

www.cpc.com/ info@cpc.com View on Map
FDA Approved Drug Records ( 28 records )
2007
27 Dec
OTC Application: 76047

Drug Name

CETIRIZINE HYDROCHLORIDE ALLERGY

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2007-12-27

76047 / 1

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Application Number

76047

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2007-12-27

Regulatory Status

OTC

2007
27 Dec
OTC Application: 76047

Drug Name

CETIRIZINE HYDROCHLORIDE ALLERGY

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2007-12-27

76047 / 2

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Application Number

76047

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2007-12-27

Regulatory Status

OTC

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

2023
20 Dec
RX Application: 217669

Drug Name

FAMOTIDINE

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2023-12-20

217669 / 1

Active Ingredient

FAMOTIDINE

Application Number

217669

Product Number

1

Dosage Form

-

Strength

20MG

Approval Date

2023-12-20

Regulatory Status

RX

2023
20 Dec
RX Application: 217669

Drug Name

FAMOTIDINE

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

2023-12-20

217669 / 2

Active Ingredient

FAMOTIDINE

Application Number

217669

Product Number

2

Dosage Form

-

Strength

40MG

Approval Date

2023-12-20

Regulatory Status

RX

2024
28 May
OTC Application: 218003

Drug Name

FAMOTIDINE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2024-05-28

218003 / 1

Active Ingredient

FAMOTIDINE

Application Number

218003

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2024-05-28

Regulatory Status

OTC

2024
28 May
OTC Application: 218003

Drug Name

FAMOTIDINE

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2024-05-28

218003 / 2

Active Ingredient

FAMOTIDINE

Application Number

218003

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2024-05-28

Regulatory Status

OTC

2026
09 Mar
RX Application: 219603

Drug Name

FAMOTIDINE

Product Number

1

Dosage Form

-

Strength

40MG/5ML

Approval Date

2026-03-09

219603 / 1

Active Ingredient

FAMOTIDINE

Application Number

219603

Product Number

1

Dosage Form

-

Strength

40MG/5ML

Approval Date

2026-03-09

Regulatory Status

RX

2025
28 Feb
OTC Application: 219032

Drug Name

FEXOFENADINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

2025-02-28

219032 / 1

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

219032

Product Number

1

Dosage Form

-

Strength

60MG

Approval Date

2025-02-28

Regulatory Status

OTC

2025
28 Feb
OTC Application: 219032

Drug Name

FEXOFENADINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

180MG

Approval Date

2025-02-28

219032 / 2

Active Ingredient

FEXOFENADINE HYDROCHLORIDE

Application Number

219032

Product Number

2

Dosage Form

-

Strength

180MG

Approval Date

2025-02-28

Regulatory Status

OTC

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

-
Unclassified Application: 71267

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

-

71267 / 1

Active Ingredient

IBUPROFEN

Application Number

71267

Product Number

1

Dosage Form

-

Strength

400MG

Approval Date

-

Regulatory Status

Unclassified

1986
15 Oct
RX Application: 71268

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1986-10-15

71268 / 1

Active Ingredient

IBUPROFEN

Application Number

71268

Product Number

1

Dosage Form

-

Strength

600MG

Approval Date

1986-10-15

Regulatory Status

RX

1986
15 Oct
RX Application: 71268

Drug Name

IBUPROFEN

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

1986-10-15

71268 / 2

Active Ingredient

IBUPROFEN

Application Number

71268

Product Number

2

Dosage Form

-

Strength

400MG

Approval Date

1986-10-15

Regulatory Status

RX

1988
01 Jul
RX Application: 71268

Drug Name

IBUPROFEN

Product Number

3

Dosage Form

-

Strength

800MG

Approval Date

1988-07-01

71268 / 3

Active Ingredient

IBUPROFEN

Application Number

71268

Product Number

3

Dosage Form

-

Strength

800MG

Approval Date

1988-07-01

Regulatory Status

RX

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

-
Unclassified Application: 72300

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

800MG

Approval Date

-

72300 / 1

Active Ingredient

IBUPROFEN

Application Number

72300

Product Number

1

Dosage Form

-

Strength

800MG

Approval Date

-

Regulatory Status

Unclassified

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
13 Jan
OTC Application: 74635

Drug Name

NAPROXEN SODIUM

Product Number

1

Dosage Form

-

Strength

220MG

Approval Date

1997-01-13

74635 / 1

Active Ingredient

NAPROXEN SODIUM

Application Number

74635

Product Number

1

Dosage Form

-

Strength

220MG

Approval Date

1997-01-13

Regulatory Status

OTC

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

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Drug Status Breakdown
28 total
  • OTC
  • Discontinued
  • RX
  • Unclassified
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

CETIRIZINE HYDROCHLORIDE ALLERGY

Application Number

76047

Product Number

1

Active Ingredient

CETIRIZINE HYDROCHLORIDE

Dosage Form

-

Strength

5MG

FDA Approved Drug Data

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