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FDAFDA · Food and drugs·Recall number D-238-2013

Tizanidine Tablets USP, 4 mg, 150-count tablets per bottle, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Bachepally - 500 090 India; NDC 55111-180-15.

Published April 10, 2013 · Recall initiated: March 19, 2013

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Labeling Illegible: There is a possibility that the bottle labels do not contain the strength of the product as well as other printing details.

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
TIZANIDINE
Manufacturer
Dr. Reddy'S Laboratories
Distributor
Nationwide and Puerto Rico.
UPC
0355111180104
Lot
Lot #: C208625, C208984, C209113, C209369, Exp 09/15; and C209680, Exp 10/15.
Risk classification
Class III
Area (FDA)
drug
Country
United States

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