RecallHawk

VALPROIC ACID

CATALENT

Summary

FDA approved VALPROIC ACID by CATALENT. ANDA (Generic) approval (Manufacturing (CMC)) on 2026-06-25. CAPSULE, ORAL.

Details

Source

Drug Approval

External ID

ANDA073229-27

Action Date

2026-06-25

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

VALPROIC ACID, CAPSULE, ORAL. Application: ANDA073229

Company

Context & Analysis

Frequently Asked Questions

How often does CATALENT have FDA actions?

This is the only FDA action we have on record for CATALENT in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "ANDA073229-27" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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