Furosemide

NDC 0143-9155 · Hikma Pharmaceuticals USA Inc.

Generic nameFurosemide

Dosage formINJECTION

RouteINTRAMUSCULAR, INTRAVENOUS

Active ingredient(s)FUROSEMIDE

Strength10 mg/mL

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

Marketing categoryNDA

Packages

0143-9155-25 — 25 VIAL, SINGLE-DOSE in 1 CARTON (0143-9155-25) / 2 mL in 1 VIAL, SINGLE-DOSE (0143-9155-01)

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

FDA lists these products with the same active ingredient.

0054-3294 — Furosemide, 0054-3298 — Furosemide, 0054-4297 — Furosemide, 0054-4299 — Furosemide, 0054-4301 — Furosemide, 0054-8297 — Furosemide, 0054-8299 — Furosemide, 0054-8301 — Furosemide, 0143-9156 — Furosemide, 0143-9157 — Furosemide, 0143-9158 — Furosemide, 0143-9159 — Furosemide, 0404-9862 — furosemide, 0404-9863 — Furosemide, 0404-9864 — furosemide, 0409-6102 — furosemide, 0615-8368 — furosemide, 0615-8369 — furosemide, 0615-8370 — furosemide, 0904-7177 — 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.