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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