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Glimepiride

NDC 50268-358 · AvPAK

Generic nameGlimepiride

Dosage formTABLET

RouteORAL

Active ingredient(s)GLIMEPIRIDE

Strength1 mg/1

Pharmacologic classSulfonylurea Compounds [CS], Sulfonylurea [EPC]

Marketing categoryANDA

Packages

50268-358-15 — 50 BLISTER PACK in 1 BOX (50268-358-15) / 1 TABLET in 1 BLISTER PACK (50268-358-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-6426 — Glimepiride, 50090-6852 — Glimepiride, 50090-6910 — Glimepiride, 50090-7187 — Glimepiride, 50090-7246 — Glimepiride, 50090-7247 — Glimepiride, 50090-7406 — Glimepiride, 50090-7407 — Glimepiride, 50090-7628 — Glimepiride, 50090-7823 — Glimepiride, 50268-359 — Glimepiride, 50268-360 — Glimepiride, 51655-120 — Glimepiride, 51655-383 — Glimepiride, 51655-489 — Glimepiride, 51655-565 — Glimepiride, 55111-320 — Glimepiride, 55111-321 — Glimepiride, 55111-322 — Glimepiride, 55154-8175 — 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