GAVIS PHARMS
FDA Approved Drugs

GAVIS PHARMS

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 1
  • Latest Approval Date Aug 02, 2002
  • Data Source FDA
  • First Approval Date Aug 02, 2002
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Company

GAVIS PHARMS

Country

U.S.A

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GAVIS PHARMS

GAVIS® Pharmaceuticals 400 Campus Drive Somerset, NJ 08873

U.S.A

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FDA Approved Drug Records ( 1 record )
2002
02 Aug
Discontinued Application: 76202

Drug Name

ACETAMINOPHEN AND PENTAZOCINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

650MG;EQ 25MG BASE

Approval Date

2002-08-02

76202 / 1

Active Ingredient

ACETAMINOPHEN; PENTAZOCINE HYDROCHLORIDE

Application Number

76202

Product Number

1

Dosage Form

-

Strength

650MG;EQ 25MG BASE

Approval Date

2002-08-02

Regulatory Status

Discontinued

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Drug Status Breakdown
1 total
  • Discontinued
Official Source

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

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FDA Approved Drug Record Details Preview

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

Drug Name

ACETAMINOPHEN AND PENTAZOCINE HYDROCHLORIDE

Application Number

76202

Product Number

1

Active Ingredient

ACETAMINOPHEN; PENTAZOCINE HYDROCHLORIDE

Dosage Form

-

Strength

650MG;EQ 25MG BASE

FDA Approved Drug Data

Approved drug product information

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