PlainRecalls
FDA Drug Moderate Class II Terminated

Lamivudine and Zidovudine Tablets USP 150mg/300mg 30 Unit Dose Blisters, Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton of 30: NDC 68084-0416-21, Individual dose: NDC 68084-0416-11

Reported: June 24, 2015 Initiated: March 2, 2015 #D-1140-2015

Product Description

Lamivudine and Zidovudine Tablets USP 150mg/300mg 30 Unit Dose Blisters, Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton of 30: NDC 68084-0416-21, Individual dose: NDC 68084-0416-11

Reason for Recall

Failed dissolution specifications

Details

Recalling Firm
American Health Packaging
Units Affected
925 cartons (30 tablets in each carton)
Distribution
Nationwide
Location
Columbus, OH

Frequently Asked Questions

What product was recalled?
Lamivudine and Zidovudine Tablets USP 150mg/300mg 30 Unit Dose Blisters, Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton of 30: NDC 68084-0416-21, Individual dose: NDC 68084-0416-11. Recalled by American Health Packaging. Units affected: 925 cartons (30 tablets in each carton).
Why was this product recalled?
Failed dissolution specifications
Which agency issued this recall?
This recall was issued by the FDA Drug on June 24, 2015. Severity: Moderate. Recall number: D-1140-2015.