US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 14, 2016 (10 years ago)

Dextroamphetamine Sulfate Tablets USP, 10 mg, 100-count bottle, Rx only, Manufactured and…

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

Why it was recalled

Failed Impurities/Degradation Specifications

What was recalled

Dextroamphetamine Sulfate Tablets USP, 10 mg, 100-count bottle, Rx only, Manufactured and Distributed by: Corepharma, LLC, Middlesex, NJ 08846, NDC 64720-0216-10

Recalling firm
Impax Laboratories, Inc.
NDC code
64720-0216-10
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0825-2016

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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