LUPIN SOMERSET recalls Hydrocodone Bitartrate and Acetaminophen Tablets, USP, 5 mg/325 mg, 1000-count bottle Rx Only, Manufactured by: Novel La
Recalled June 6, 2018 · FDA recall D-0836-2018 · LUPIN SOMERSET
Hazard
Labeling: Missing Label · FDA Class III
Units
1,672 (1000-count) bottles
Sold at
OH
Description
Labeling: Missing Label
Product
Hydrocodone Bitartrate and Acetaminophen Tablets, USP, 5 mg/325 mg, 1000-count bottle Rx Only, Manufactured by: Novel Laboratories, Inc. Somerset NJ 08873 Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 212020 NDC 43386-356-10 UPC 343386356102
Manufacturer(s)
LUPIN SOMERSET
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →