US Drug Recall Register
Class II · Moderate risk Terminated Initiated Feb 16, 2016 (11 years ago)

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed Impurities/Degradation Specifications: Out of specification for impurities.

What was recalled

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 30 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: 45963-749-11.

Recalling firm
Actavis Elizabeth LLC
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0815-2016

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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