Drug recall D-0148-2024
Product
Penicillamine Tablets USP 250 mg, 100-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202 Manufactured by: Lupin Limited, Nagpur-441 108, India, NDC# 70748-153-01
Reason for recall
Failed Dissolution Specifications
Lots and codes
Lot # M200498, Exp. June 2024
Recall details
- Recalling firm
- Lupin Pharmaceuticals Inc., Baltimore, MD
- Quantity
- N/A
- Distribution
- Product was distributed to 3 wholesale/distributor accounts.
- Type
- Voluntary: Firm initiated
- Recall initiated
- November 22, 2023
- Terminated
- July 8, 2024
Related products
- Penicillamine – drug information
- NDC 70748-153 Penicillamine · Penicillamine 250 mg/1 · Lupin Pharmaceuticals, Inc.