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Class II · ModerateRecall completed

Atenolol

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

Does this affect you?
Check your lot numberMP2292 Exp. 01/16
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

Superpotent Drug: A complaint was reported by a pharmacist who stated several tablets were noticeably thicker in appearance.

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 byCadila Healthcare Ltd. Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08634 USA foreign manufacturer
Brand nameATENOLOL
Generic nameATENOLOL
Active ingredient(s)ATENOLOL
Distributed by / forZydus Pharmaceuticals USA Inc. Pennington, NJ 08634 USA
NDC68382-022-01
Show the full FDA record
Full product labelZyGenerics ATENOLOL Tablets, USP 25 mg 1000 count bottle, Rx Only Manufactured by: Cadila Healthcare Ltd. Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08634 USA NDC 68382-022-01
Recalling firmZydus Pharmaceuticals USA Inc
DistributionNationwide
Quantity5400 bottles
Recall initiated2014-08-05
Report date2014-10-15
Recall completed2017-09-22
Recall numberD-0007-2015
ClassificationClass II
FDA statusTerminated
Origin on filePennington NJ United States

Related

Atenolol recallsRecent drug recallsCheck another medication

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.