Is Hydrocodone Bitartrate and Acetaminophen Tablets, USP, 5 mg/500 mg C-III; an Rx oral schedule C-III narcotic analgesic and antitussive; Manufactured by Able Laboratories, Inc., South Plainfield, NJ 07080, Packaged and Distributed by UDL Laboratories, Inc., Rockford, IL 61103; single tablet unit dose packs, NDC #51079-420-20: 10 sheets of 10 unit dose tablets, NDC #51079-420-21: 5 sheets of 20 unit dose tablets, NDC #51079-420-99: 15 sheets of 6 unit dose tablets recalled?

Question

Is Hydrocodone Bitartrate and Acetaminophen Tablets, USP, 5 mg/500 mg C-III; an Rx oral schedule C-III narcotic analgesic and antitussive; Manufactured by Able Laboratories, Inc., South Plainfield, NJ 07080, Packaged and Distributed by UDL Laboratories, Inc., Rockford, IL 61103; single tablet unit dose packs,  NDC #51079-420-20: 10 sheets of 10 unit dose tablets, NDC #51079-420-21: 5 sheets of 20 unit dose tablets, NDC #51079-420-99: 15 sheets of 6 unit dose tablets recalled?

Accepted Answer

The drug products repackaged by UDL were recalled by the manufacturer, Able Laboratories due to a lack of assurance that testing conducted for release and stability conformed to standard operating procedures.

Distribution: Nationwide

UDL Laboratories, Inc.: The drug products repackaged by UDL were recalled by the manufacturer, Able Laboratories due to a lack of assurance that testing conducted for release and stability conformed to standard operating procedures.

Additional Information

Were You Affected by This Recall?

UDL Laboratories, Inc.: The drug products repackaged by UDL were recalled by the manufacturer, Able Laboratories due to a lack of assurance that testing conducted for release and stability conformed to standard operating procedures.

Additional Information

Were You Affected by This Recall?