US Drug Recall Register
Class III · Low risk Terminated Initiated Apr 10, 2019 (7 years ago)

Morphine Sulfate Extended-Release Tablets, 60 mg, 100-count bottles, Rx Only…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Impurities/Degradation Specifications

What was recalled

Morphine Sulfate Extended-Release Tablets, 60 mg, 100-count bottles, Rx Only, Manufactured by: Novel Laboratories, Inc. Somerset, NJ 08873 Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202 NDC 43386-542-01

Recalling firm
Lupin Somerset
NDC code
43386-542-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1245-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Morphine recalls

See all