WhichRecall
Class IIReported 2025-09-17

Chlorpromazine Hydrochloride Tablets, USP, 200 mg, 100-count bottle, Rx only, Manufactured By: Zydus Lifesciences Ltd., Baddi, India; Manufactured for: Northstar Rx LLC Memphis, TN 38141. NDC: 16714-051-01

Recalled by Zydus Pharmaceuticals (USA) Inc

Reason for Recall

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

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Recall Number
D-0639-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-09-03
Reported
2025-09-17
Distribution
Nationwide in the USA
Code Info
Lot #: Z305085, Exp Date 30-09-25; Z401166, Z401167, Exp Date 28-02-26
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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