Reported Jul 27, 2022 · Ongoing

Aspirin and Extended-Release Dipyridamole Capsules, 25mg/200 mg, 60-count bottle, Rx Only, Manufactured for: Glenmark…

Glenmark Pharmaceuticals Inc., USA

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

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: Glenmark Pharmaceuticals Inc., USA · 750 Corporate Dr · Mahwah, NJ · 07430-2009

Is this the product you have?

  • Aspirin and Extended-Release Dipyridamole Capsules, 25mg/200 mg, 60-count bottle, Rx Only
  • Manufactured forGlenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, Product of India, NDC 68462-405-60
Lot codes and dates
    • Lot#: 17201639
    • Exp 08/2022
    • 17201759
    • Exp 09/2022
    • 17202067
    • Exp 10/2022
    • 17210696
    • Exp 02/2023
    • 17210092
    • Exp 11/2022
    • 17210145
    • Exp 12/2022
    • 17210732
    • Exp 02/2023
    • 17211062
    • Exp 04/2023
    • 17211441
    • Exp 05/2023
    • 17211670
    • Exp 06/2023
    • 17211810
    • Exp 07/2023
    • 17211862
    • 17212020
    • 17212068
    • Exp 08/2023
    • 17212438
    • Exp 10/2023
    • 17220172
    • 17220251
    • Exp 12/2023
Amount recalled
168936 bottles

Where it was sold

  • Nationwide

Why it was recalled

Failed Tablet/Capsule Specification : Capsule breakage

This product is unlikely to cause harm, but it breaks a safety or labelling rule.

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Where this came from

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

Read the FDA (openFDA drug enforcement) notice

Data as of Sep 19, 6:37 PM UTC

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