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Glimepiride

NDC 68084-788 · American Health Packaging

Generic nameGlimepiride

Dosage formTABLET

RouteORAL

Active ingredient(s)GLIMEPIRIDE

Strength1 mg/1

Pharmacologic classSulfonylurea Compounds [CS], Sulfonylurea [EPC]

Marketing categoryANDA

Packages

68084-788-25 — 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-788-25) / 1 TABLET in 1 BLISTER PACK (68084-788-95)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

66993-822 — pioglitazone and glimepiride, 67046-1608 — Glimepiride, 68001-584 — Glimepiride, 68001-585 — Glimepiride, 68001-586 — Glimepiride, 68071-2228 — Glimepiride, 68071-2385 — Glimepiride, 68071-3639 — Glimepiride, 68084-326 — Glimepiride, 68084-327 — Glimepiride, 68788-8432 — Glimepiride, 68788-8728 — Glimepiride, 70518-4485 — Glimepiride, 70518-4486 — Glimepiride, 71205-773 — Glimepiride, 71205-779 — Glimepiride, 71335-0180 — Glimepiride, 71335-0484 — Glimepiride, 71335-1885 — Glimepiride, 71335-1886 — 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