# FDA recall D-0144-2017

> **Amerisource Health Services** · Class III · drug recall initiated 2016-10-13.

## 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

## Distribution

US

## Key facts

- **Recall number:** D-0144-2017
- **Recalling firm:** Amerisource Health Services
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-10-13
- **Report date:** 2016-11-30
- **Termination date:** 2017-09-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Columbus, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0144-2017

## Citation

> AI Analytics. FDA recall D-0144-2017. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0144-2017. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*