AHP NIFEdipine Capsules, 10mg USP, 100 count carton (NDC: 68084-022-01); Individual Blister (NDC:...

FDA Recall #D-0144-2017 — Class III — October 13, 2016

Recall #D-0144-2017 Date: October 13, 2016 Classification: Class III Status: Terminated

Product Description

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

Reason for Recall

Presence of Foreign Tablets/Capsules

Recalling Firm

Amerisource Health Services — Columbus, OH

Classification

Class III — Not likely to cause adverse health consequences.

Product Type

Drugs

Product Quantity

5283 cartons (100 capsules per carton = 528,300 capsules)

Distribution

US

Code Information

Lot #155404 ; Exp 01/18 Lot #161139,163060,164054, 164809; Exp 03/18

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated