Contract Pharmacal Corporation OTC
FDA Approved Drugs

Contract Pharmacal Corporation OTC

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
  • Total Records 7
  • Latest Approval Date Feb 28, 2025
  • Data Source FDA
  • First Approval Date Jan 13, 1997
All
28
View
Unclassified
2
View
Discontinued
13
View
OTC
7
View
RX
6
View
Company Overview

Company

Contract Pharmacal Corporation OTC

Country

U.S.A

Social Profiles

LinkedIn
Company Snapshot

Contract Pharmacal Corporation OTC

165 Oser Avenue Hauppauge, NY 11788

U.S.A

www.cpc.com/ info@cpc.com View on Map
FDA Approved Drug Records ( 7 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

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

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

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

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Drug Status Breakdown
7 total
  • OTC
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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