FUROSEMIDE

NDC 59651-796 · Aurobindo Pharma Limited

Generic nameFUROSEMIDE

Dosage formTABLET

RouteORAL

Active ingredient(s)FUROSEMIDE

Strength20 mg/1

Pharmacologic classIncreased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]

Marketing categoryANDA

Packages

59651-796-01 — 100 TABLET in 1 BOTTLE (59651-796-01)

59651-796-99 — 1000 TABLET in 1 BOTTLE (59651-796-99)

FDA lists these products with the same active ingredient.

55150-322 — Furosemide, 55150-323 — Furosemide, 55150-324 — Furosemide, 55154-2348 — furosemide, 55154-2349 — furosemide, 55154-2364 — Furosemide, 55154-2365 — FUROSEMIDE, 55154-4452 — furosemide, 55154-9581 — FUROSEMIDE, 55154-9582 — FUROSEMIDE, 59651-797 — FUROSEMIDE, 59651-798 — FUROSEMIDE, 60760-858 — Furosemide, 61919-242 — FUROSEMIDE, 61919-255 — Furosemide, 62135-753 — Furosemide, 62135-754 — Furosemide, 63187-506 — Furosemide, 63187-517 — Furosemide, 63187-739 — Furosemide, +194 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.