Contract Pharmacal Corporation RX
FDA Approved Drugs

Contract Pharmacal Corporation RX

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.

RX
  • Total Records 6
  • Latest Approval Date Mar 09, 2026
  • Data Source FDA
  • First Approval Date Oct 15, 1986
All
28
View
Unclassified
2
View
Discontinued
13
View
OTC
7
View
RX
6
View
Company Overview

Company

Contract Pharmacal Corporation RX

Country

U.S.A

Social Profiles

LinkedIn
Company Snapshot

Contract Pharmacal Corporation RX

165 Oser Avenue Hauppauge, NY 11788

U.S.A

www.cpc.com/ info@cpc.com View on Map
FDA Approved Drug Records ( 6 records )
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

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

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

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Drug Status Breakdown
6 total
  • 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

FAMOTIDINE

Application Number

217669

Product Number

1

Active Ingredient

FAMOTIDINE

Dosage Form

-

Strength

20MG

FDA Approved Drug Data

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