AHP NIFEdipine Capsules — Class III drug recall D-0144-2017
Terminated recall by Amerisource Health Services, reported 2016-11-30. Presence of Foreign Tablets/Capsules
| Recall number | D-0144-2017 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Amerisource Health Services, Columbus, OH, United States |
| Recall initiated | 2016-10-13 |
| Classified | 2016-11-18 |
| Reported by FDA | 2016-11-30 |
| Terminated | 2017-09-28 |
| NDC | 68084-0022-01, 68084-0022-11 |
| Lot numbers | 01/18, 03/18, 155404, 161139, 163060, 164054, 164809 |
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
Reason for recall
Presence of Foreign Tablets/Capsules
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0144-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.