FDAFDA · Food and drugs·Recall number D-0046-2015
GLIMEPIRIDE TABLETS, USP 2 mg, a)100 count bottle, (NDC 42571-101-01), b) 500 count Bottle (NDC 42571-101-05), Rx only, Manufactured by: Micro Labs Limited, Goa-403 722, INDIA, Manufactured for: Micro Labs USA, Inc., Princeton, NJ 08540
Published November 5, 2014 · Recall initiated: October 9, 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 Stability Specifications: Micro Labs is recalling two lots due to out of specification results during stability testing.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- GLIMEPIRIDE
- Manufacturer
- Micro Labs Usa, Inc S
- Distributor
- CT, FL, MD, MS, NY
- UPC
- 0342571100018
- Lot
- GLBG001 Exp.12/14, GLBG008 Exp. 06/15
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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