NDC 71335-0150 – Glyburide

Glyburide 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0150

Product details

Brand name
Glyburide
Generic name
Glyburide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090937
Marketed since
October 5, 2010
Listing expires
December 31, 2026
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glyburide →

Package NDC codes (6)

Package NDCDescriptionSince
71335-0150-130 TABLET in 1 BOTTLE (71335-0150-1)Sep 4, 2018
71335-0150-2120 TABLET in 1 BOTTLE (71335-0150-2)Jan 28, 2025
71335-0150-3100 TABLET in 1 BOTTLE (71335-0150-3)Jan 28, 2025
71335-0150-460 TABLET in 1 BOTTLE (71335-0150-4)Jul 23, 2018
71335-0150-590 TABLET in 1 BOTTLE (71335-0150-5)May 23, 2018
71335-0150-6180 TABLET in 1 BOTTLE (71335-0150-6)Feb 12, 2021

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