NDC 71335-0180 – Glimepiride

Glimepiride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0180

Product details

Brand name
Glimepiride
Generic name
Glimepiride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078181
Marketed since
August 23, 2007
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glimepiride →

Package NDC codes (5)

Package NDCDescriptionSince
71335-0180-130 TABLET in 1 BOTTLE (71335-0180-1)Dec 19, 2014
71335-0180-260 TABLET in 1 BOTTLE (71335-0180-2)Dec 19, 2014
71335-0180-390 TABLET in 1 BOTTLE (71335-0180-3)Dec 19, 2014
71335-0180-4180 TABLET in 1 BOTTLE (71335-0180-4)Dec 19, 2014
71335-0180-5100 TABLET in 1 BOTTLE (71335-0180-5)Apr 5, 2024

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