RecallHawk

Summary

FDA approved ADAPALENE by ACTAVIS MID ATLANTIC. ANDA (Generic) approval (Labeling) on 2024-08-26. GEL, TOPICAL.

Details

Source

Drug Approval

External ID

ANDA201000-7

Action Date

2024-08-26

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

ADAPALENE, GEL, TOPICAL. Application: ANDA201000

Context & Analysis

ACTAVIS MID ATLANTIC has 6 FDA actions in our database.

Frequently Asked Questions

How often does ACTAVIS MID ATLANTIC have FDA actions?

ACTAVIS MID ATLANTIC has 6 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 "ANDA201000-7" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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