NDC 72162-2215 – Glipizide

Glipizide 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72162-2215

Product details

Brand name
Glipizide
Generic name
Glipizide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074497
Marketed since
December 13, 2021
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glipizide →

Package NDC codes (1)

Package NDCDescriptionSince
72162-2215-01000 TABLET in 1 BOTTLE (72162-2215-0)Aug 27, 2026

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