NDC 71335-9655 – Glimepiride

Glimepiride 1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-9655

Product details

Brand name
Glimepiride
Generic name
Glimepiride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202759
Marketed since
June 29, 2012
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glimepiride →

Package NDC codes (5)

Package NDCDescriptionSince
71335-9655-130 TABLET in 1 BOTTLE (71335-9655-1)Mar 28, 2023
71335-9655-260 TABLET in 1 BOTTLE (71335-9655-2)Apr 13, 2026
71335-9655-390 TABLET in 1 BOTTLE (71335-9655-3)Mar 10, 2023
71335-9655-4100 TABLET in 1 BOTTLE (71335-9655-4)Mar 17, 2023
71335-9655-520 TABLET in 1 BOTTLE (71335-9655-5)Apr 13, 2026

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