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Furosemide

NDC 63561-0164 · Granulation Technology, Inc.

Generic nameFUROSEMIDE
Dosage formTABLET
RouteORAL
Active ingredient(s)FUROSEMIDE
Strength20 mg/1
Pharmacologic classIncreased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
Marketing categoryNDA

Packages

63561-0164-1 — 100 TABLET in 1 BOTTLE (63561-0164-1)

63561-0164-2 — 1000 TABLET in 1 BOTTLE (63561-0164-2)

63561-0164-9 — 90 TABLET in 1 BOTTLE (63561-0164-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60760-858 — Furosemide, 61919-242 — FUROSEMIDE, 61919-255 — Furosemide, 62135-753 — Furosemide, 62135-754 — Furosemide, 63187-506 — Furosemide, 63187-517 — Furosemide, 63187-739 — Furosemide, 63187-790 — Furosemide, 63323-280 — FUROSEMIDE, 63561-0165 — FUROSEMIDE, 63561-0166 — FUROSEMIDE, 63629-1119 — furosemide, 63629-1120 — furosemide, 63629-1214 — furosemide, 63629-1215 — furosemide, 63629-1216 — furosemide, 63629-1217 — furosemide, 64980-562 — Furosemide, 64980-563 — 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.