NDC 68788-4178 – Glipizide

Glipizide 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-4178

Product details

Brand name
Glipizide
Generic name
Glipizide
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074378
Marketed since
July 31, 2026
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glipizide →

Package NDC codes (5)

Package NDCDescriptionSince
68788-4178-1100 TABLET in 1 BOTTLE (68788-4178-1)Jul 31, 2026
68788-4178-330 TABLET in 1 BOTTLE (68788-4178-3)Jul 31, 2026
68788-4178-660 TABLET in 1 BOTTLE (68788-4178-6)Jul 31, 2026
68788-4178-8180 TABLET in 1 BOTTLE (68788-4178-8)Jul 31, 2026
68788-4178-990 TABLET in 1 BOTTLE (68788-4178-9)Jul 31, 2026

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