Actavis Elizabeth LLC recalls Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 20 mg,
Recalled April 13, 2016 · FDA recall D-0814-2016 · Actavis Elizabeth
Hazard
Failed Impurities/Degradation Specifications: Out of specification for impurities. · FDA Class II
Units
257,746 Bottles
Sold at
US: Nationwide
Description
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 20 mg, 100 ct. bottle, Rx Only. Manufactured by: Actavis Elizabeth LLC, Elmora Avenue, Elizabeth, NJ 07207. Distributed by: Actavis, Inc., 80 Columbia Road, Bldg B, Morristown, NJ 07960. NDC: 45963-748-11.
Manufacturer(s)
Actavis Elizabeth LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →