Watson Laboratories Inc recalls Hydrocodone Bitartrate and Acetaminophen Tablets USP, 10 mg/500 mg, 500-count Tablets per bottle, Rx only, Manufactured
Recalled November 28, 2012 · FDA recall D-058-2013 · Watson Laboratories
Hazard
Superpotent (Multiple Ingredient) Drug: There is the potential for oversized and superpotent tablets. · FDA Class I
Units
4,874 bottles
Sold at
Nationwide
Description
Superpotent (Multiple Ingredient) Drug: There is the potential for oversized and superpotent tablets.
Product
Hydrocodone Bitartrate and Acetaminophen Tablets USP, 10 mg/500 mg, 500-count Tablets per bottle, Rx only, Manufactured By: Watson Laboratories, Inc., Corona, CA 92880 USA, NDC 00591-0540-05.
Manufacturer(s)
Watson Laboratories Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →