ALLERGAN recalls NORCO (Hydrocodone Bitartrate and Acetaminophen) Tablets, USP, 10 mg/325 mg, 100-count bottles, Rx Only, Distributed by:

Recalled February 21, 2018 · FDA recall D-0413-2018 · ALLERGAN

Hazard

Labeling: Not Elsewhere Classified: does not have the required "CII" controlled drug classification indication on the primary label. · FDA Class III

Units

8 bottles

Sold at

Nationwide in the USA

Description

Labeling: Not Elsewhere Classified: does not have the required "CII" controlled drug classification indication on the primary label.

Product

NORCO (Hydrocodone Bitartrate and Acetaminophen) Tablets, USP, 10 mg/325 mg, 100-count bottles, Rx Only, Distributed by: Allergan USA, Inc., Irvine, CA 92612, NDC 0023-6022-01.

Manufacturer(s)

ALLERGAN

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →