NDC 71335-9742 – Glipizide

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

Human Prescription Drug

Product NDC71335-9742

Product details

Brand name
Glipizide
Generic name
Glipizide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA206928
Marketed since
March 3, 2023
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glipizide →

Package NDC codes (4)

Package NDCDescriptionSince
71335-9742-190 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-1)Apr 9, 2026
71335-9742-230 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-2)Jun 26, 2023
71335-9742-360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-3)Apr 9, 2026
71335-9742-4100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9742-4)Jul 14, 2023

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