Major ChlorproMAZINE Hydrochloride Tablets, USP, 50 mg, 100 Tablets, (10x10) blister package, Rx ...

FDA Recall #D-0011-2026 — Class II — September 12, 2025

Recall #D-0011-2026 Date: September 12, 2025 Classification: Class II Status: Ongoing

Product Description

Major ChlorproMAZINE Hydrochloride Tablets, USP, 50 mg, 100 Tablets, (10x10) blister package, Rx Only, Packaged and Distributed by Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-7131-61, UPC (01)00309047131617

Reason for Recall

CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit

Recalling Firm

The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories — La Vergne, TN

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

506 blister packs

Distribution

Nationwide

Code Information

Lots N02009 & N02026, exp. date 02/28/2026

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated