FDA Drug recall 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: Mi…

FDA Drug
Class II
terminated
Published 2014-11-05

On 2014-11-05 the FDA classified a Class II recall of 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: Mi… by Micro Labs Usa S, citing failed Stability Specifications: Micro Labs is recalling two lots due to out of specification results during stability testing.

Read the official FDA Drug notice

Agency	FDA Drug
Recall number	D-0046-2015
Classification	Class II
Status	terminated
Initiated	2014-10-09
Published	2014-11-05
Last updated	2026-09-13 11:51 UTC
Company	Micro Labs Usa S
Distribution	CT, FL, MD, MS, NY

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

Reason

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

Identifiers

ndc	42571-100-01
ndc	42571-100-05
ndc	42571-101-01
ndc	42571-101-05
ndc	42571-102-01
ndc	42571-102-05
ndc	42571-103-01
ndc	42571-103-05
ndc	42571-104-01
ndc	42571-104-05
ndc	42571-105-01
ndc	42571-105-05
code_info	GLBG001 Exp.12/14, GLBG008 Exp. 06/15

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0046-2015%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.