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Class II · ModerateActive recall

Chlorpromazine Hydrochloride

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot #: Z306326, Exp Date 30-11-25; Z401155, Exp Date 28-02-26
Where it was soldNationwide in the USA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

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

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byZydus Lifesciences Ltd., Baddi, India; Manufactured for: Northstar Rx LLC Memphis, TN 38141 foreign manufacturer
Brand nameCHLORPROMAZINE HYDROCHLORIDE
Generic nameCHLORPROMAZINE HYDROCHLORIDE
Active ingredient(s)CHLORPROMAZINE HYDROCHLORIDE
Distributed by / forNorthstar Rx LLC Memphis, TN 38141
NDC16714-049-01
Show the full FDA record
Full product labelChlorpromazine Hydrochloride Tablets, USP, 50 mg, 100-count bottle, Rx only, Manufactured By: Zydus Lifesciences Ltd., Baddi, India; Manufactured for: Northstar Rx LLC Memphis, TN 38141. NDC: 16714-049-01
Recalling firmZydus Pharmaceuticals (USA) Inc
DistributionNationwide in the USA
QuantityN/A
Recall initiated2025-09-03
Report date2025-09-17
Recall completed—
Recall numberD-0635-2025
ClassificationClass II
FDA statusOngoing
Origin on filePennington NJ United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.