LUPIN SOMERSET recalls Nitrofurantoin Oral Suspension USP, 25mg/5mL, 230 mL Bottle, Rx Only, Manufactured by: Novel Laboratories, Inc. Somerset
Recalled July 18, 2018 · FDA recall D-0927-2018 · LUPIN SOMERSET
Hazard
Subpotent Drug and Failed Content Uniformity. · FDA Class II
Units
3456 cartons
Sold at
Nationwide within the US
Description
Subpotent Drug and Failed Content Uniformity.
Product
Nitrofurantoin Oral Suspension USP, 25mg/5mL, 230 mL Bottle, Rx Only, Manufactured by: Novel Laboratories, Inc. Somerset, NJ 08873, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202, UPC 343386-450-114, NDC 43386-450-11
Manufacturer(s)
LUPIN SOMERSET
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →