NDC 71335-0618 – Glipizide

Glipizide 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0618

Product details

Brand name
Glipizide
Generic name
Glipizide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075795
Marketed since
September 25, 2002
Listing expires
December 31, 2026
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glipizide →

Package NDC codes (7)

Package NDCDescriptionSince
71335-0618-160 TABLET in 1 BOTTLE (71335-0618-1)Mar 20, 2018
71335-0618-230 TABLET in 1 BOTTLE (71335-0618-2)Mar 1, 2018
71335-0618-3100 TABLET in 1 BOTTLE (71335-0618-3)Feb 19, 2018
71335-0618-4120 TABLET in 1 BOTTLE (71335-0618-4)Oct 8, 2024
71335-0618-590 TABLET in 1 BOTTLE (71335-0618-5)Feb 16, 2018
71335-0618-620 TABLET in 1 BOTTLE (71335-0618-6)Oct 8, 2024
71335-0618-7180 TABLET in 1 BOTTLE (71335-0618-7)Apr 10, 2018

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