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FUROSEMIDE

NDC 61919-242 · DIRECT RX

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

61919-242-30 — 30 TABLET in 1 BOTTLE (61919-242-30)

61919-242-90 — 90 TABLET in 1 BOTTLE (61919-242-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55154-2349 — furosemide, 55154-2364 — Furosemide, 55154-2365 — FUROSEMIDE, 55154-4452 — furosemide, 55154-9581 — FUROSEMIDE, 55154-9582 — FUROSEMIDE, 59651-796 — FUROSEMIDE, 59651-797 — FUROSEMIDE, 59651-798 — FUROSEMIDE, 60760-858 — Furosemide, 61919-255 — Furosemide, 62135-753 — Furosemide, 62135-754 — Furosemide, 63187-506 — Furosemide, 63187-517 — Furosemide, 63187-739 — Furosemide, 63187-790 — Furosemide, 63323-280 — FUROSEMIDE, 63561-0164 — FUROSEMIDE, 63561-0165 — 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels