AHP NIFEdipine Capsules recall
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
Why was AHP NIFEdipine Capsules recalled?
Presence of Foreign Tablets/Capsules
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #155404 ; Exp 01/18 Lot #161139,163060,164054, 164809; Exp 03/18
- Product
- 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
- Recalling firm
- Amerisource Health Services
- Quantity
- 5283 cartons (100 capsules per carton = 528,300 capsules)
- Distribution
- US
- Recall date
- November 30, 2016
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)