Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals recalls Hydrocodone bitartrate and acetaminophen Tablets, USP, 10 mg/500 mg, packaged in a) 30-count bottles, NDC 0603-3888-16;
Recalled February 6, 2013 · FDA recall D-138-2013 · Vintage Pharmaceuticals LLC
Hazard
Superpotent (Multiple Ingredient) Drug: Complaint received of oversized tablets. · FDA Class I
Units
897,379 bottles
Sold at
Nationwide and Puerto Rico
Description
Superpotent (Multiple Ingredient) Drug: Complaint received of oversized tablets.
Product
Hydrocodone bitartrate and acetaminophen Tablets, USP, 10 mg/500 mg, packaged in a) 30-count bottles, NDC 0603-3888-16; b) 60-count bottles, NDC 0603-3888-20; c) 90-count bottles, NDC 0603-3888-02; d) 100-count bottles, NDC 0603-3888-21; e) 120-count bottles, NDC 0603-3888-22; f) 150-count bottles, NDC 0603-3888-26; g) 180-count bottles, NDC 0603-3888-04; h) 500-count bottles, NDC 0603-3888-28; and i) 1000-count bottles, NDC 0603-3888-32, Rx only, Mfg. for: Qualitest Pharmaceuticals, Huntsville, AL 35811.
Manufacturer(s)
Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →