Class II · Moderate riskOngoing 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.