Reported Apr 27, 2016 · Terminated

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

Impax Laboratories, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Impax Laboratories, Inc. · 215 Wood Ave · Middlesex, NJ · 08846-2554

Is this the product you have?

  • Dextroamphetamine Sulfate Tablets USP, 10 mg, 100-count bottle, Rx only
  • Manufactured and Distributed byCorepharma, LLC, Middlesex, NJ 08846, NDC 64720-0216-10
Lot codes and dates
    • Lot # 112579
    • 112580
    • Exp 03/17
    • 111013A
    • Exp 04/16
    • 111014
    • Exp 05/16
    • 113292
    • 113332
    • 113386
    • 113387
    • Exp 07/17
    • 111671
    • 111673
    • Exp 09/16
    • 113806
    • 113807
    • Exp 10/17
    • 111874
    • 111875
    • 111876
    • Exp 11/16
Amount recalled
67,428 bottles

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

Failed Impurities/Degradation Specifications

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Feb 9, 2018 · Data as of Sep 19, 5:48 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.