NDC 71335-2561 – Glimepiride

Glimepiride 1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2561

Product details

Brand name
Glimepiride
Generic name
Glimepiride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202112
Marketed since
July 31, 2023
Listing expires
December 31, 2026
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glimepiride →

Package NDC codes (5)

Package NDCDescriptionSince
71335-2561-130 TABLET in 1 BOTTLE (71335-2561-1)Jan 28, 2025
71335-2561-260 TABLET in 1 BOTTLE (71335-2561-2)Jan 28, 2025
71335-2561-390 TABLET in 1 BOTTLE (71335-2561-3)Jan 28, 2025
71335-2561-4100 TABLET in 1 BOTTLE (71335-2561-4)Jan 28, 2025
71335-2561-520 TABLET in 1 BOTTLE (71335-2561-5)Jan 28, 2025

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