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Furosemide

NDC 70518-4679 · REMEDYREPACK INC.

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

70518-4679-0 — 30 TABLET in 1 BLISTER PACK (70518-4679-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70121-1076 — Furosemide, 70121-1163 — Furosemide, 70121-1164 — Furosemide, 70518-0050 — Furosemide, 70518-0251 — Furosemide, 70518-2528 — Furosemide, 70518-3061 — furosemide, 70518-3757 — Furosemide, 70518-4444 — furosemide, 70518-4609 — furosemide, 70756-618 — furosemide, 70756-619 — furosemide, 70756-620 — furosemide, 71288-203 — Furosemide, 71335-0384 — Furosemide, 71335-0842 — furosemide, 71335-0852 — furosemide, 71335-2317 — Furosemide, 71335-2319 — Furosemide, 71610-049 — 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.