FDAFebruary 2, 2018drug

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Terminated

Brands named

allergan

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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