FDAFDA · Food and drugs·Recall number D-0326-2015
Alprazolam tablets, USP, CIV, 0.25 mg, Rx Only, a) 500 count bottle, b) 1000 count bottle, Distributed by: Greenstone LLC, Peapack, NJ, 07977, a) NDC 59762-3719-3, b) NDC 59762-3719-4.
Published December 31, 2014 · Recall initiated: December 17, 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
Subpotent Drug
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- ALPRAZOLAM
- Manufacturer
- Neolpharma, Inc.
- Distributor
- Nationwide
- Lot
- Lot #: a) C100429, Exp 03/15, b) C120293, Exp 01/17
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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