Skip to main content

Glimepiride

NDC 68001-584 · BluePoint Laboratories

Generic nameGlimepiride
Dosage formTABLET
RouteORAL
Active ingredient(s)GLIMEPIRIDE
Strength1 mg/1
Pharmacologic classSulfonylurea Compounds [CS], Sulfonylurea [EPC]
Marketing categoryANDA

Packages

68001-584-00 — 100 TABLET in 1 BOTTLE (68001-584-00)

68001-584-03 — 500 TABLET in 1 BOTTLE (68001-584-03)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63187-698 — Glimepiride, 63629-3043 — Glimepiride, 64764-302 — pioglitazone and glimepiride, 64764-304 — pioglitazone and glimepiride, 65862-579 — Glimepiride, 65862-580 — Glimepiride, 65862-581 — Glimepiride, 66993-821 — pioglitazone and glimepiride, 66993-822 — pioglitazone and glimepiride, 67046-1608 — Glimepiride, 68001-585 — Glimepiride, 68001-586 — Glimepiride, 68071-2228 — Glimepiride, 68071-2385 — Glimepiride, 68071-3639 — Glimepiride, 68084-326 — Glimepiride, 68084-327 — Glimepiride, 68084-788 — Glimepiride, 68788-8432 — Glimepiride, 68788-8728 — 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.