FDA Drug Low Class III Terminated

AHP NIFEdipine Capsules, 10mg USP, 100 count carton (NDC: 68084-022-01); Individual Blister (NDC: 68084-022-11), Rx Only, Manufactured by: Actavis Elizabeth, LLC, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217

Reported: November 30, 2016 Initiated: October 13, 2016 #D-0144-2017

Product Description

Reason for Recall

Presence of Foreign Tablets/Capsules

Details

Recalling Firm: Amerisource Health Services
Units Affected: 5283 cartons (100 capsules per carton = 528,300 capsules)
Distribution: US
Location: Columbus, OH

Frequently Asked Questions

What product was recalled? ▼

AHP NIFEdipine Capsules, 10mg USP, 100 count carton (NDC: 68084-022-01); Individual Blister (NDC: 68084-022-11), Rx Only, Manufactured by: Actavis Elizabeth, LLC, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217. Recalled by Amerisource Health Services. Units affected: 5283 cartons (100 capsules per carton = 528,300 capsules).

Why was this product recalled? ▼

Presence of Foreign Tablets/Capsules

Which agency issued this recall? ▼

This recall was issued by the FDA Drug on November 30, 2016. Severity: Low. Recall number: D-0144-2017.