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Class II · ModerateRecall completed

Metoprolol Succinate

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot # C206578 Exp. 05/2014 Lot # C207415 Exp. 06/2014
Where it was soldNationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

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

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byDr. Reddy's Laboratories Limited, Batchupally - 500 090 India foreign manufacturer
Brand nameMETOPROLOL SUCCINATE
Generic nameMETOPROLOL SUCCINATE
Active ingredient(s)METOPROLOL SUCCINATE
Distributed by / forDr. Reddy's Laboratories, Inc.
NDC55111-466-01
Show the full FDA record
Full product labelDr. 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 firmDr. Reddy's Laboratories, Inc.
DistributionNationwide
Quantity13560 bottles
Recall initiated2014-05-23
Report date2014-06-18
Recall completed2015-05-01
Recall numberD-1381-2014
ClassificationClass II
FDA statusTerminated
Origin on filePrinceton NJ United States

Related

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Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.