NDC 71335-2353 – Glipizide

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

Human Prescription Drug

Product NDC71335-2353

Product details

Brand name
Glipizide
Generic name
Glipizide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA206928
Marketed since
March 3, 2023
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glipizide →

Package NDC codes (5)

Package NDCDescriptionSince
71335-2353-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2353-1)Feb 21, 2024
71335-2353-260 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2353-2)Feb 21, 2024
71335-2353-3100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2353-3)Feb 21, 2024
71335-2353-490 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2353-4)Feb 21, 2024
71335-2353-5180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2353-5)Feb 21, 2024

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