Major ChlorproMAZINE Hydrochloride Tablets recalled over manufacturing violations
- Recall date
- September 12, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories recalls Major ChlorproMAZINE Hydrochloride Tablets, USP, 25 mg, 50 Tablets (5x10) blister package, Rx Only, Packaged and Di…
- Recall number
- D-0009-2026
- FDA classification
- Class II
- Brand / firm
- The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories
- Sold / distributed
- Nationwide
Why it was recalled
CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Major ChlorproMAZINE Hydrochloride Tablets, USP, 25 mg, 50 Tablets (5x10) blister package, Rx Only, Packaged and Distributed by Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-7130-06, UPC (01)00309047130061
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