Reported Mar 27, 2013 · Terminated

Carisoprodol Tablets, USP, 350 mg Rx Only, 100 tablets per bottle, Rx Only, Manufactured by: West-ward Pharmaceutical…

West-ward Pharmaceutical Corp.

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: West-ward Pharmaceutical Corp. · 465 Industrial Way W · Eatontown, NJ · 07724-2209

Is this the product you have?

  • Carisoprodol Tablets, USP, 350 mg Rx Only, 100 tablets per bottle, Rx Only
  • Manufactured byWest-ward Pharmaceutical Corp., Eatontown, NJ 07724, NDC 0143-1176-01
Lot codes and dates
  • Lot #: 69160A
Amount recalled
1763 bottles

Where it was sold

  • Nationwide

Why it was recalled

Labeling: Not elsewhere classified: On 12/12/11, DEA published a final rule in the Federal Register making this product a schedule IV (C-IV)controlled substance. This product is being recalled because this controlled product was not relabeled with the required "C-IV" imprint on the label for products distributed after the 06/11/12 deadline.

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

Notice updated Dec 18, 2014 · Data as of Sep 19, 5:02 PM UTC

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