NDC 68788-4061 – Glipizide

Glipizide 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-4061

Product details

Brand name
Glipizide
Generic name
Glipizide
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074378
Marketed since
January 28, 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
68788-4061-1100 TABLET in 1 BOTTLE (68788-4061-1)Jan 28, 2026
68788-4061-330 TABLET in 1 BOTTLE (68788-4061-3)Jan 28, 2026
68788-4061-660 TABLET in 1 BOTTLE (68788-4061-6)Jan 28, 2026
68788-4061-8180 TABLET in 1 BOTTLE (68788-4061-8)Jan 28, 2026
68788-4061-990 TABLET in 1 BOTTLE (68788-4061-9)Jan 28, 2026

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