NDC 42571-104 – Glimepiride

Glimepiride 6 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC42571-104

Product details

Brand name
Glimepiride
Generic name
Glimepiride
Labeler
Micro Labs Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091220
Marketed since
June 13, 2013
Listing expires
December 31, 2026
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glimepiride →

Package NDC codes (2)

Package NDCDescriptionSince
42571-104-01100 TABLET in 1 BOTTLE (42571-104-01)Jun 13, 2013
42571-104-05500 TABLET in 1 BOTTLE (42571-104-05)Jun 13, 2013

Recalls mentioning this NDC

Other Glimepiride products