FDAFDA · Food and drugs·Recall number D-0639-2025
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
Published September 17, 2025 · Recall initiated: September 3, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
What to do
Voluntary: Firm initiated
Recall details
- Brand
- CHLORPROMAZINE HYDROCHLORIDE
- Manufacturer
- Zydus Pharmaceuticals (USA) Inc
- Distributor
- Nationwide in the USA
- Lot
- Lot #: Z305085, Exp Date 30-09-25; Z401166, Z401167, Exp Date 28-02-26
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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