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Furosemide

NDC 69315-118 · Leading Pharma, LLC

Generic nameFurosemide
Dosage formTABLET
RouteORAL
Active ingredient(s)FUROSEMIDE
Strength80 mg/1
Pharmacologic classIncreased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
Marketing categoryANDA

Packages

69315-118-01 — 100 TABLET in 1 BOTTLE (69315-118-01)

69315-118-05 — 500 TABLET in 1 BOTTLE (69315-118-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68083-433 — Furosemide, 68083-434 — Furosemide, 68094-756 — Furosemide, 68094-867 — Furosemide, 68788-6784 — Furosemide, 68788-6948 — Furosemide, 68788-8799 — Furosemide, 68788-8870 — Furosemide, 69315-116 — Furosemide, 69315-117 — Furosemide, 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, +194 more

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