Lupin Pharmaceuticals Inc. recalls Penicillamine Tablets USP 250 mg, 100-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD
Recalled December 20, 2023 · FDA recall D-0148-2024 · Lupin Pharmaceuticals
Hazard
Failed Dissolution Specifications · FDA Class II
Units
N/A
Sold at
Product was distributed to 3 wholesale/distributor accounts.
Description
Failed Dissolution Specifications
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
Manufacturer(s)
Lupin Pharmaceuticals Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →