Furosemide

NDC 83980-002 · Ipca Laboratories Limited

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

83980-002-01 — 100 TABLET in 1 BOTTLE (83980-002-01)

83980-002-10 — 1000 TABLET in 1 BOTTLE (83980-002-10)

83980-002-97 — 10 TABLET in 1 BOTTLE (83980-002-97)

FDA lists these products with the same active ingredient.

72603-474 — Furosemide, 72789-030 — furosemide, 72789-032 — furosemide, 72789-033 — furosemide, 72789-157 — furosemide, 73043-022 — furosemide, 73043-023 — furosemide, 73043-024 — furosemide, 73542-101 — Furosemide, 73542-102 — Furosemide, 73542-103 — Furosemide, 81137-001 — furosemide, 81565-201 — FUROSEMIDE, 82868-050 — Furosemide, 83634-302 — furosemide, 83980-003 — Furosemide, 83980-004 — Furosemide, 84549-251 — Furosemide, 84549-474 — Furosemide, 87441-033 — 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.