FUROSEMIDE

NDC 51662-1574 · HF Acquisition Co LLC, DBA HealthFirst

Generic nameFUROSEMIDE

Dosage formINJECTION, SOLUTION

RouteINTRAMUSCULAR, INTRAVENOUS

Active ingredient(s)FUROSEMIDE

Strength10 mg/mL

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

Marketing categoryNDA

Packages

51662-1574-1 — 4 mL in 1 VIAL (51662-1574-1)

51662-1574-3 — 25 POUCH in 1 CASE (51662-1574-3) / 1 VIAL in 1 POUCH (51662-1574-2) / 4 mL in 1 VIAL

J1938 — Injection, furosemide, 1 mg Medicare Part B payment limit (ASP + 6%): $0.02

FDA lists these products with the same active ingredient.

50090-7706 — Furosemide, 50090-7708 — Furosemide, 51655-269 — furosemide, 51655-310 — furosemide, 51655-481 — Furosemide, 51655-517 — furosemide, 51662-1226 — FUROSEMIDE, 51662-1227 — FUROSEMIDE, 51662-1336 — FUROSEMIDE, 51662-1572 — FUROSEMIDE, 51662-1575 — FUROSEMIDE, 55150-322 — Furosemide, 55150-323 — Furosemide, 55150-324 — Furosemide, 55154-2348 — furosemide, 55154-2349 — furosemide, 55154-2364 — Furosemide, 55154-2365 — FUROSEMIDE, 55154-4452 — furosemide, 55154-9581 — FUROSEMIDE, +194 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.