NDC 16729-002 – Glimepiride

Glimepiride 2 mg/1 · Tablet · Oral

Human Prescription Drug 3 recalls

Product NDC16729-002

Product details

Brand name
Glimepiride
Generic name
Glimepiride
Labeler
Accord Healthcare Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078181
Marketed since
August 23, 2007
Listing expires
December 31, 2026
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glimepiride →

Package NDC codes (2)

Package NDCDescriptionSince
16729-002-01100 TABLET in 1 BOTTLE (16729-002-01)Aug 23, 2007
16729-002-16500 TABLET in 1 BOTTLE (16729-002-16)Aug 24, 2016

Recalls mentioning this NDC

Other Glimepiride products