PlainRecalls
FDA Drug Moderate Class II Terminated

Zebeta¿ (bisoprolol fumarate), tablets, 10mg, 30-count bottle, Rx only, Manufactured for Teva Pharmaceuticals Inc. 425 Privet Road, Horsham, PA by Duramed Pharmaceuticals, Inc., a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY 10970 for Teva. NDC 51285-061-01

Reported: June 10, 2015 Initiated: May 11, 2015 #D-1112-2015

Product Description

Zebeta¿ (bisoprolol fumarate), tablets, 10mg, 30-count bottle, Rx only, Manufactured for Teva Pharmaceuticals Inc. 425 Privet Road, Horsham, PA by Duramed Pharmaceuticals, Inc., a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY 10970 for Teva. NDC 51285-061-01

Reason for Recall

Failed Dissolution Specifications: OOS result during stability testing

Details

Recalling Firm
Teva Pharmaceuticals USA
Units Affected
889 bottles
Distribution
Nationwide
Location
Horsham, PA

Frequently Asked Questions

What product was recalled?
Zebeta¿ (bisoprolol fumarate), tablets, 10mg, 30-count bottle, Rx only, Manufactured for Teva Pharmaceuticals Inc. 425 Privet Road, Horsham, PA by Duramed Pharmaceuticals, Inc., a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY 10970 for Teva. NDC 51285-061-01. Recalled by Teva Pharmaceuticals USA. Units affected: 889 bottles.
Why was this product recalled?
Failed Dissolution Specifications: OOS result during stability testing
Which agency issued this recall?
This recall was issued by the FDA Drug on June 10, 2015. Severity: Moderate. Recall number: D-1112-2015.