Furosemide

NDC 42571-436 · Micro Labs Limited

Generic nameFurosemide

Dosage formINJECTION

RouteINTRAMUSCULAR, INTRAVENOUS

Active ingredient(s)FUROSEMIDE

Strength20 mg/2mL

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

Marketing categoryANDA

Packages

42571-436-87 — 25 VIAL in 1 CARTON (42571-436-87) / 2 mL in 1 VIAL (42571-436-75)

FDA lists these products with the same active ingredient.

31722-311 — Furosemide, 36000-063 — furosemide, 36000-064 — furosemide, 36000-065 — furosemide, 36000-282 — furosemide, 36000-283 — furosemide, 36000-284 — furosemide, 42291-468 — furosemide, 42291-469 — furosemide, 42291-470 — furosemide, 42571-437 — Furosemide, 42571-438 — Furosemide, 42708-123 — Furosemide, 43063-702 — Furosemide, 43063-716 — Furosemide, 43063-849 — furosemide, 43353-069 — Furosemide, 43353-747 — Furosemide, 43547-401 — furosemide, 43547-402 — 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.