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Glipizide

NDC 72162-2103 · Bryant Ranch Prepack

Generic nameGlipizide

Dosage formTABLET

RouteORAL

Active ingredient(s)GLIPIZIDE

Strength5 mg/1

Pharmacologic classSulfonylurea Compounds [CS], Sulfonylurea [EPC]

Marketing categoryANDA

Packages

72162-2103-0 — 1000 TABLET in 1 BOTTLE (72162-2103-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2528 — Glipizide, 71335-2540 — Glipizide, 71335-3133 — Glipizide, 71335-9614 — Glipizide, 71335-9742 — Glipizide, 71610-105 — Glipizide, 71610-175 — Glipizide, 71610-668 — Glipizide, 71610-680 — Glipizide, 72162-2102 — Glipizide, 72162-2215 — Glipizide, 72162-2614 — Glipizide, 72789-130 — Glipizide, 72789-463 — Glipizide, 72789-464 — Glipizide, 72789-510 — Glipizide, 72888-115 — Glipizide, 72888-116 — Glipizide, 72888-117 — Glipizide, 72888-231 — Glipizide, +132 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels