US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Feb 6, 2025 (2 years ago)

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

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed Dissolution Specifications

What was recalled

Morphine Sulfate Extended-Release Tablets, 100 mg, 100-count bottles, Rx Only, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901. Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512. NDC 63304-452-01

Recalling firm
Sun Pharmaceutical Industries INC
NDC code
63304-452-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0249-2025

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.

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