NDC 71335-3133 – Glipizide

Glipizide 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3133

Product details

Brand name
Glipizide
Generic name
Glipizide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074378
Marketed since
May 1, 2025
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glipizide →

Package NDC codes (7)

Package NDCDescriptionSince
71335-3133-1100 TABLET in 1 BOTTLE (71335-3133-1)May 21, 2026
71335-3133-230 TABLET in 1 BOTTLE (71335-3133-2)May 21, 2026
71335-3133-360 TABLET in 1 BOTTLE (71335-3133-3)May 21, 2026
71335-3133-490 TABLET in 1 BOTTLE (71335-3133-4)May 21, 2026
71335-3133-520 TABLET in 1 BOTTLE (71335-3133-5)May 21, 2026
71335-3133-6180 TABLET in 1 BOTTLE (71335-3133-6)May 21, 2026
71335-3133-710 TABLET in 1 BOTTLE (71335-3133-7)May 21, 2026

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