Actavis Elizabeth LLC recalls NIFEdipine Capsules USP, 10 mg, Rx only, 100 count bottle, Manufactured and distributed by: Actavis Elizabeth LLC, 200…
- Recall date
- October 6, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0143-2017
- FDA classification
- Class III
- Brand / firm
- Actavis Elizabeth LLC
- Sold / distributed
- US
Why it was recalled
Presence of Foreign Tablets/Capsules
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
NIFEdipine Capsules USP, 10 mg, Rx only, 100 count bottle, Manufactured and distributed by: Actavis Elizabeth LLC, 200 Elmora Avenue, Elizabeth, NJ 07207, NDC 0228-2407-10
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