RecallWatchUSA

Home / Recalls / Drugs

Valeant Pharmaceuticals North America LLC recalls Lodrane D (Brompheniramine maleate 4 mg and Pseudoephedrine HCl 60 mg) Capsules, 60-count bottles, Distributed by: Valea

Recalled June 22, 2016 · FDA recall D-1032-2016 · Valeant Pharmaceuticals North America

Hazard
Labeling: Not Elsewhere Classified: correctly labeled bottles were packaged in cartons that were mislabeled with an incorrect active ingredient, phenylephrine rather than pseudoephedrine, on the carton face and carton top. · FDA Class III
Units
3827 bottles
Sold at
Nationwide

Description

Labeling: Not Elsewhere Classified: correctly labeled bottles were packaged in cartons that were mislabeled with an incorrect active ingredient, phenylephrine rather than pseudoephedrine, on the carton face and carton top.

Product
Lodrane D (Brompheniramine maleate 4 mg and Pseudoephedrine HCl 60 mg) Capsules, 60-count bottles, Distributed by: Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807, UPC 0 00950 86006 8.
Manufacturer(s)
Valeant Pharmaceuticals North America LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Valeant Pharmaceuticals North America LLC recalls Lodrane D (Brompheniramine maleate 4 mg and Pseudoephedrine HCl 60 mg) Capsules, 60-count bottles, Distributed by: Valea | RecallWatchUSA