NDC 51655-966 – Glipizide

Glipizide 10 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC51655-966

Product details

Brand name
Glipizide
Generic name
Glipizide
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA204720
Marketed since
June 27, 2023
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glipizide →

Package NDC codes (2)

Package NDCDescriptionSince
51655-966-2690 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-966-26)Jul 31, 2023
51655-966-5230 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-966-52)Jun 27, 2023

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