FDAFDA · Food and drugs·Recall number D-1091-2014
Alprazolam Extended-Release Tablets, USP, 3 mg, 60-count tablets per bottle, Rx only, Manufactured by: Actavis Elizabeth LLC, 200 Elmora Avenue, Elizabeth, NJ 07207, NDC 0228-3086-06, UPC 3 0228-3086-06 2.
Published March 12, 2014 · Recall initiated: February 4, 2014
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
Failed Dissolution Specifications: Product did not meet specification requirements for dissolution.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Actavis Elizabeth LLC
- Distributor
- Nationwide
- Lot
- Lot #: 57617531, Exp 03/14
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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