PlainRecalls
FDA Drug Low Class III Terminated

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.

Reported: February 21, 2018 Initiated: February 2, 2018 #D-0413-2018

Product Description

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.

Reason for Recall

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

Details

Recalling Firm
ALLERGAN
Units Affected
8 bottles
Distribution
Nationwide in the USA
Location
Madison, NJ

Frequently Asked Questions

What product was recalled?
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.. Recalled by ALLERGAN. Units affected: 8 bottles.
Why was this product recalled?
Labeling: Not Elsewhere Classified: does not have the required "CII" controlled drug classification indication on the primary label.
Which agency issued this recall?
This recall was issued by the FDA Drug on February 21, 2018. Severity: Low. Recall number: D-0413-2018.