RecallHawk

BACLOFEN

IMPAX

Summary

FDA approved BACLOFEN by IMPAX. ANDA (Generic) approval (Labeling) on 2022-04-19. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA077971-3

Action Date

2022-04-19

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

BACLOFEN, TABLET, ORAL. Application: ANDA077971

Company

Context & Analysis

IMPAX has 4 FDA actions in our database.

Frequently Asked Questions

How often does IMPAX have FDA actions?

IMPAX has 4 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 "ANDA077971-3" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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