Reported Jul 1, 2026 · Ongoing · Updated Sep 16, 2026

Fenofibrate Capsules, USP 200 mg, Rx only, 100 Capsules, Manufactured by: Ajanta Pharma Limited, India, Marketed by:…

Ajanta Pharma USA 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: Ajanta Pharma USA Inc · 400 Crossing Blvd Ste 102 · Bridgewater, NJ · 08807-2863

Is this the product you have?

  • Fenofibrate Capsules, USP 200 mg, Rx only, 100 Capsules
  • Manufactured byAjanta Pharma Limited, India
  • Marketed by
    • Ajanta Pharma USA Inc. Bridgewater
    • NJ 08807
    • NDC 27241-120-04
Lot codes and dates
    • Lot # PA02216
    • Exp. 12/2029
Amount recalled
3648 bottles

Where it was sold

  • Nationwide

Why it was recalled

CGMP Deviations

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

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Where this came from

Source: U.S. Food & Drug Administration (Enforcement Report)

Read the FDA (weekly enforcement report) notice

Data as of Sep 19, 4:55 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.