NDC 51655-337 – Glipizide

Glipizide 5 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC51655-337

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
May 26, 2020
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glipizide →

Package NDC codes (1)

Package NDCDescriptionSince
51655-337-2690 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-337-26)May 26, 2020

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