Furosemide

NDC 0054-4301 · Hikma Pharmaceuticals USA Inc.

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

0054-4301-25 — 100 TABLET in 1 BOTTLE, PLASTIC (0054-4301-25)

0054-4301-29 — 500 TABLET in 1 BOTTLE, PLASTIC (0054-4301-29)

FDA lists these products with the same active ingredient.

0054-3294 — Furosemide, 0054-3298 — Furosemide, 0054-4297 — Furosemide, 0054-4299 — Furosemide, 0054-8297 — Furosemide, 0054-8299 — Furosemide, 0054-8301 — Furosemide, 0143-9155 — 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 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.