Teva Pharmaceuticals USA recalls DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE Tablets, (CII), 1
Recalled November 5, 2014 · FDA recall D-0050-2015 · Teva Pharmaceuticals USA
Hazard
Failed Impurities/Degradation Specifications: Out of specification for unknown impurities. · FDA Class II
Units
19,545 Bottles
Sold at
U.S. Nationwide including Puerto Rico.
Description
Failed Impurities/Degradation Specifications: Out of specification for unknown impurities.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE Tablets, (CII), 10 mg, 100 Tablet Bottles, Rx Only. Teva Pharmaceuticals USA , Sellersville, PA 18960, NDC: 0555-0972-02. 0555-0972-02, lot #s 34016373A, 34016377A, exp. dated 7/2016.
Manufacturer(s)
Teva Pharmaceuticals USA
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →