RecallHawk

Summary

FDA approved METAXALONE by ACTAVIS LABS FL INC. ANDA (Generic) approval (Labeling) on 2024-11-07. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA203695-6

Action Date

2024-11-07

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

METAXALONE, TABLET, ORAL. Application: ANDA203695

Context & Analysis

ACTAVIS LABS FL INC has 17 FDA actions in our database.

Frequently Asked Questions

How often does ACTAVIS LABS FL INC have FDA actions?

ACTAVIS LABS FL INC has 17 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 "ANDA203695-6" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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