NDC 71335-1886 – Glimepiride

Glimepiride 2 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1886

Product details

Brand name
Glimepiride
Generic name
Glimepiride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091220
Marketed since
June 13, 2013
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glimepiride →

Package NDC codes (5)

Package NDCDescriptionSince
71335-1886-130 TABLET in 1 BOTTLE (71335-1886-1)Dec 21, 2021
71335-1886-260 TABLET in 1 BOTTLE (71335-1886-2)Dec 21, 2021
71335-1886-390 TABLET in 1 BOTTLE (71335-1886-3)Dec 21, 2021
71335-1886-4100 TABLET in 1 BOTTLE (71335-1886-4)Dec 21, 2021
71335-1886-5180 TABLET in 1 BOTTLE (71335-1886-5)Dec 21, 2021

Other Glimepiride products