US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Sep 17, 2025 (12 months ago)

Azelaic Acid Gel, 15%, 50 grams, For Topical Use Only, Rx only, Manufactured by: Glenmark…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations: Market complaints received for gritty texture (grainy)

What was recalled

Azelaic Acid Gel, 15%, 50 grams, For Topical Use Only, Rx only, Manufactured by: Glenmark Pharmaceuticals Limited Colvale-Bardez, Goa 403513, India, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, NDC 68462-626-52

Recalling firm
Glenmark Pharmaceuticals Inc., USA
NDC code
68462-626-52
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0662-2025

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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