Furosemide

NDC 70518-0251 · REMEDYREPACK INC.

Generic nameFurosemide

Dosage formTABLET

RouteORAL

Active ingredient(s)FUROSEMIDE

Strength40 mg/1

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

Marketing categoryANDA

Packages

70518-0251-1 — 90 TABLET in 1 BOTTLE, PLASTIC (70518-0251-1)

70518-0251-3 — 30 TABLET in 1 BLISTER PACK (70518-0251-3)

FDA lists these products with the same active ingredient.

68788-6948 — Furosemide, 68788-8799 — Furosemide, 68788-8870 — Furosemide, 69315-116 — Furosemide, 69315-117 — Furosemide, 69315-118 — Furosemide, 70121-1076 — Furosemide, 70121-1163 — Furosemide, 70121-1164 — Furosemide, 70518-0050 — Furosemide, 70518-2528 — Furosemide, 70518-3061 — furosemide, 70518-3757 — Furosemide, 70518-4444 — furosemide, 70518-4609 — furosemide, 70518-4679 — Furosemide, 70756-618 — furosemide, 70756-619 — furosemide, 70756-620 — furosemide, 71288-203 — Furosemide, +194 more

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