Anchen Pharmaceutical, Inc
FDA Approved Drugs

Anchen Pharmaceutical, Inc

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.

Unclassified Discontinued
  • Total Records 5
  • Latest Approval Date Mar 16, 2012
  • Data Source FDA
  • First Approval Date Mar 16, 2012
All
5
View
Unclassified
2
View
Discontinued
3
View
Company Overview

Company

Anchen Pharmaceutical, Inc

Country

U.S.A

Website

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Company Snapshot

Anchen Pharmaceutical, Inc

300 Tice Boulevard Woodcliff Lake, NJ 07677, USA

U.S.A

www.parpharm.com/ View on Map
FDA Approved Drug Records ( 5 records )
-
Unclassified Application: 204009

Drug Name

DESVENLAFAXINE

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

-

204009 / 1

Active Ingredient

DESVENLAFAXINE

Application Number

204009

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 204009

Drug Name

DESVENLAFAXINE

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

-

204009 / 2

Active Ingredient

DESVENLAFAXINE

Application Number

204009

Product Number

2

Dosage Form

-

Strength

100MG

Approval Date

-

Regulatory Status

Unclassified

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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  • FDA Approved Drugs Database
    5 View
Drug Status Breakdown
5 total
  • Unclassified
  • Discontinued
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

DESVENLAFAXINE

Application Number

204009

Product Number

1

Active Ingredient

DESVENLAFAXINE

Dosage Form

-

Strength

50MG

FDA Approved Drug Data

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