Actavis Elizabeth LLC recalls Dextroamphetamine Sulfate Extended-Release Capsules, 15 mg, 90-count bottles, Rx Only, Manufactured by: Actavis Elizabe
Recalled March 11, 2015 · FDA recall D-0395-2015 · Actavis Elizabeth
Hazard
Failed Dissolution Specifications · FDA Class II
Units
42 bottles
Sold at
Nationwide
Description
Failed Dissolution Specifications
Product
Dextroamphetamine Sulfate Extended-Release Capsules, 15 mg, 90-count bottles, Rx Only, Manufactured by: Actavis Elizabeth LLC, Elizabeth, NJ 07201 USA; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054 USA; NDC 45963-305-09, UPC 3 45963-305-09 1.
Manufacturer(s)
Actavis Elizabeth LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →