NDC 68788-4017 – Glipizide

Glipizide 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-4017

Product details

Brand name
Glipizide
Generic name
Glipizide
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214874
Marketed since
August 29, 2025
Listing expires
December 31, 2026
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glipizide →

Package NDC codes (5)

Package NDCDescriptionSince
68788-4017-1100 TABLET in 1 BOTTLE (68788-4017-1)Aug 29, 2025
68788-4017-330 TABLET in 1 BOTTLE (68788-4017-3)Aug 29, 2025
68788-4017-660 TABLET in 1 BOTTLE (68788-4017-6)Aug 29, 2025
68788-4017-818 TABLET in 1 BOTTLE (68788-4017-8)Aug 29, 2025
68788-4017-990 TABLET in 1 BOTTLE (68788-4017-9)Aug 29, 2025

Other Glipizide products