US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Oct 6, 2025 (11 months ago)

Desipramine Hydrochloride Tablets, USP, 10 mg, 100 - count bottle (NDC 23155-578-01), Rx…

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

Why it was recalled

CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.

What was recalled

Desipramine Hydrochloride Tablets, USP, 10 mg, 100 - count bottle (NDC 23155-578-01), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816.

Recalling firm
Heritage Pharmaceuticals Inc
NDC code
23155-578-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0107-2026

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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