Micro Labs Usa, Inc S recalls GLIMEPIRIDE TABLETS, USP 2 mg, a)100 count bottle, (NDC 42571-101-01), b) 500 count Bottle (NDC 42571-101-05), Rx only,

Recalled November 5, 2014 · FDA recall D-0046-2015 · Micro Labs Usa, Inc S

Hazard

Failed Stability Specifications: Micro Labs is recalling two lots due to out of specification results during stability testing. · FDA Class II

Units

11,328 bottles

Sold at

CT, FL, MD, MS, NY

Description

Failed Stability Specifications: Micro Labs is recalling two lots due to out of specification results during stability testing.

Product

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

Manufacturer(s)

Micro Labs Usa, Inc S

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →