Reported Apr 16, 2025 · Ongoing

Pravastatin Sodium Tablets, 20mg, a).500-count bottle (NDC# 68462-196-05), b). 90-count bottle (NDC# 68462-196-90), Rx…

Glenmark Pharmaceuticals Inc., USA

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

Is this the product you have?

    • Pravastatin Sodium Tablets
    • 20mg
    • a).500-count bottle (NDC# 68462-196-05)
    • b). 90-count bottle (NDC# 68462-196-90)
    • Rx only
  • Manufactured byGlenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, India
  • Manufactured forGlenmark Pharmaceuticals Inc. USA, Mahwah, NJ 07430
Lot codes and dates
    • Lot # 17230810
    • exp. date Mar-26 17230811
    • exp. date Mar-26 17230810
    • exp. date Mar-26 17232501
    • exp. date Nov-26 17232502
    • exp. date Nov-26
Amount recalled
N/A

This recall covers 39 products

The agency filed one notice per product. You are reading one of them; the other 38 are below.

26 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

CGMP Deviations

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

Want the full recall guide?

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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, 7:22 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.