Actavis Inc recalls Dextroamphetamine Sulfate Extended-Release Capsules, 10 mg, 90- count bottles, Rx Only Manufactured by: Actavis Elizabet
Recalled August 3, 2016 · FDA recall D-1448-2016 · Actavis
Hazard
Failed Dissolution Specifications · FDA Class II
Units
8,062 units
Sold at
Nationwide
Description
Failed Dissolution Specifications
Product
Dextroamphetamine Sulfate Extended-Release Capsules, 10 mg, 90- count bottles, Rx Only Manufactured by: Actavis Elizabeth LLC Elizabeth, NJ 07207 USA; Distributed by: Actavis Pharma, Inc Parsippany, NJ 07054 USA NDC 45963-304-09
Manufacturer(s)
Actavis Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →