FDAFDA · Food and drugs·Recall number D-0542-2025
Amlodipine and Benazepril HCl Capsules USP 2.5 mg/10 mg, 100 Capsules bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL, 34108, United States, Manufactured by: Lupin Limited, Goa 103 722, INDIA, NDC 68180-755-01.
Published August 6, 2025 · Recall initiated: July 2, 2025
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling: Incorrect or Missing Lot and/or Exp Date: released with wrong expiry date as Feb.2027 instead of Jan.2027
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
- Manufacturer
- Lupin Pharmaceuticals Inc.
- Distributor
- Nationwide in the US
- UPC
- 0368180459019
- Lot
- Lot GB01616, expiration 2/28/2027
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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