US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 13, 2013 (13 years ago)

Dr. Reddy's Metoprolol Succinate Extended-Release Tablets USP, 50 mg 100 tablets Rx Only…

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

Why it was recalled

Failed Dissolution Specification; 12-Month stability interval.

What was recalled

Dr. Reddy's Metoprolol Succinate Extended-Release Tablets USP, 50 mg 100 tablets Rx Only Mfd. By: Dr. Reddy's Laboratories Limited Bachepalli -500 090 INDIA NDC 55111-467-01

Recalling firm
Dr. Reddy's Laboratories, Inc.
NDC code
55111-467-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1080-2014

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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