NDC 71335-1031 – Glipizide

Glipizide 5 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC71335-1031

Product details

Brand name
Glipizide
Generic name
Glipizide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA204720
Marketed since
April 24, 2017
Listing expires
December 31, 2026
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glipizide →

Package NDC codes (4)

Package NDCDescriptionSince
71335-1031-190 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1031-1)Jan 7, 2019
71335-1031-230 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1031-2)Jan 7, 2019
71335-1031-360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1031-3)Jan 7, 2019
71335-1031-4100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1031-4)Jan 7, 2019

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