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Furosemide

NDC 51655-310 · Northwind Health Company, LLC

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

51655-310-53 — 10 TABLET in 1 BOTTLE, PLASTIC (51655-310-53)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-6646 — Furosemide, 50090-6647 — Furosemide, 50090-6937 — Furosemide, 50090-6942 — Furosemide, 50090-7703 — Furosemide, 50090-7704 — Furosemide, 50090-7705 — Furosemide, 50090-7706 — Furosemide, 50090-7708 — Furosemide, 51655-269 — furosemide, 51655-481 — Furosemide, 51655-517 — furosemide, 51662-1226 — FUROSEMIDE, 51662-1227 — FUROSEMIDE, 51662-1336 — FUROSEMIDE, 51662-1572 — FUROSEMIDE, 51662-1574 — FUROSEMIDE, 51662-1575 — FUROSEMIDE, 55150-322 — Furosemide, 55150-323 — 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.