Anchen Pharmaceutical, Inc Discontinued
FDA Approved Drugs

Anchen Pharmaceutical, Inc 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 3
  • Latest Approval Date Mar 16, 2012
  • Data Source FDA
  • First Approval Date Mar 16, 2012
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Unclassified
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Discontinued
3
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Company Overview

Company

Anchen Pharmaceutical, Inc Discontinued

Country

U.S.A

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Company Snapshot

Anchen Pharmaceutical, Inc Discontinued

300 Tice Boulevard Woodcliff Lake, NJ 07677, USA

U.S.A

www.parpharm.com/ View on Map
FDA Approved Drug Records ( 3 records )
2012
16 Mar
Discontinued Application: 78087

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 37.5MG BASE

Approval Date

2012-03-16

78087 / 1

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

78087

Product Number

1

Dosage Form

-

Strength

EQ 37.5MG BASE

Approval Date

2012-03-16

Regulatory Status

Discontinued

2012
16 Mar
Discontinued Application: 78087

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2012-03-16

78087 / 2

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

78087

Product Number

2

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2012-03-16

Regulatory Status

Discontinued

2012
16 Mar
Discontinued Application: 78087

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

2012-03-16

78087 / 3

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

78087

Product Number

3

Dosage Form

-

Strength

EQ 150MG BASE

Approval Date

2012-03-16

Regulatory Status

Discontinued

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Drug Status Breakdown
3 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

VENLAFAXINE HYDROCHLORIDE

Application Number

78087

Product Number

1

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Dosage Form

-

Strength

EQ 37.5MG BASE

FDA Approved Drug Data

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