NDC 71335-0967 – Glyburide and Metformin Hydrochloride

Glyburide 5 mg/1; Metformin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0967

Product details

Brand name
Glyburide and Metformin Hydrochloride
Generic name
Glyburide and Metformin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077870
Marketed since
November 14, 2007
Listing expires
December 31, 2026
Pharmacologic class
Biguanide; Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glyburide and Metformin Hydrochloride →

Package NDC codes (7)

Package NDCDescriptionSince
71335-0967-130 TABLET, FILM COATED in 1 BOTTLE (71335-0967-1)Oct 15, 2018
71335-0967-360 TABLET, FILM COATED in 1 BOTTLE (71335-0967-3)Oct 15, 2018
71335-0967-490 TABLET, FILM COATED in 1 BOTTLE (71335-0967-4)May 30, 2024
71335-0967-5120 TABLET, FILM COATED in 1 BOTTLE (71335-0967-5)May 30, 2024
71335-0967-6100 TABLET, FILM COATED in 1 BOTTLE (71335-0967-6)Oct 11, 2018
71335-0967-7180 TABLET, FILM COATED in 1 BOTTLE (71335-0967-7)May 30, 2024
71335-0967-825 TABLET, FILM COATED in 1 BOTTLE (71335-0967-8)May 30, 2024

Other Glyburide and Metformin Hydrochloride products