Reported Aug 14, 2013 · Terminated

Rifadin, Rifampin capsules, 150 mg, packaged in 30-count bottle, Rx only, Mfd. for Sanofi-Aventis, U.S., LLC,…

Sanofi US

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: Sanofi US · 55 Corporate Dr · Bridgewater, NJ · 08807-1265

Is this the product you have?

  • Rifadin, Rifampin capsules, 150 mg, packaged in 30-count bottle, Rx only, Mfd. for Sanofi-Aventis, U.S., LLC, Bridgewater, NJ 08807, NDC 0068-0510-30
Lot codes and dates
    • Lot # 3097657
    • Exp 3/15
Amount recalled
2,462 bottles

Where it was sold

  • Nationwide

Why it was recalled

Subpotent drug: low fill volume in some of the capsules

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 (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Mar 17, 2014 · Data as of Sep 19, 7:16 PM UTC

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