US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 23, 2014 (12 years ago)

Dr. Reddy's Metoprolol Succinate Extended Release Tablets, USP 25 mg. 100-count bottle…

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

Why it was recalled

Failed Dissolution Specifications: Failure of dissolution test observed at the 18 month time point.

What was recalled

Dr. Reddy's Metoprolol Succinate Extended Release Tablets, USP 25 mg. 100-count bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories Limited, Batchupally - 500 090 India. NDC55111-466-01

Recalling firm
Dr. Reddy's Laboratories, Inc.
NDC code
55111-466-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1381-2014

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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