RecallHawk

VENLAFAXINE HYDROCHLORIDE

PHARMADAX

Summary

FDA approved VENLAFAXINE HYDROCHLORIDE by PHARMADAX. ANDA (Generic) approval on 2022-01-04. TABLET, EXTENDED RELEASE, ORAL.

Details

Source

Drug Approval

External ID

ANDA214423-1

Action Date

2022-01-04

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

VENLAFAXINE HYDROCHLORIDE, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA214423

Company

Context & Analysis

PHARMADAX has 3 FDA actions in our database.

Frequently Asked Questions

How often does PHARMADAX have FDA actions?

PHARMADAX has 3 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "ANDA214423-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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