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Glimepiride

NDC 72189-485 · Direct_Rx

Generic nameGlimepiride
Dosage formTABLET
RouteORAL
Active ingredient(s)GLIMEPIRIDE
Strength2 mg/1
Pharmacologic classSulfonylurea Compounds [CS], Sulfonylurea [EPC]
Marketing categoryANDA

Packages

72189-485-30 — 30 TABLET in 1 BOTTLE (72189-485-30)

72189-485-60 — 60 TABLET in 1 BOTTLE (72189-485-60)

72189-485-90 — 90 TABLET in 1 BOTTLE (72189-485-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-0180 — Glimepiride, 71335-0484 — Glimepiride, 71335-1885 — Glimepiride, 71335-1886 — Glimepiride, 71335-2367 — Glimepiride, 71335-2409 — Glimepiride, 71335-2561 — Glimepiride, 71335-9654 — Glimepiride, 71335-9655 — Glimepiride, 71610-236 — Glimepiride, 71921-214 — Glimepiride, 71921-215 — Glimepiride, 71921-216 — Glimepiride, 72189-585 — Glimepiride, 72336-641 — Glimepiride, 72789-048 — Glimepiride, 72789-370 — Glimepiride, 82804-065 — Glimepiride, 82804-140 — Glimepiride, 82868-042 — Glimepiride, +86 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