Skip to main content

Furosemide

NDC 71335-2319 · Bryant Ranch Prepack

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

71335-2319-0 6 TABLET in 1 BOTTLE (71335-2319-0)

71335-2319-1 30 TABLET in 1 BOTTLE (71335-2319-1)

71335-2319-2 90 TABLET in 1 BOTTLE (71335-2319-2)

71335-2319-3 60 TABLET in 1 BOTTLE (71335-2319-3)

71335-2319-4 100 TABLET in 1 BOTTLE (71335-2319-4)

71335-2319-5 7 TABLET in 1 BOTTLE (71335-2319-5)

71335-2319-6 28 TABLET in 1 BOTTLE (71335-2319-6)

71335-2319-7 14 TABLET in 1 BOTTLE (71335-2319-7)

71335-2319-8 10 TABLET in 1 BOTTLE (71335-2319-8)

71335-2319-9 20 TABLET in 1 BOTTLE (71335-2319-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4609 — furosemide, 70518-4679 — Furosemide, 70756-618 — furosemide, 70756-619 — furosemide, 70756-620 — furosemide, 71288-203 — Furosemide, 71335-0384 — Furosemide, 71335-0842 — furosemide, 71335-0852 — furosemide, 71335-2317 — Furosemide, 71610-049 — furosemide, 71610-096 — furosemide, 71610-634 — furosemide, 71610-635 — furosemide, 71610-636 — furosemide, 71610-843 — Furosemide, 71610-951 — Furosemide, 71767-100 — furosemide injection 80 mg/ 10 mL, 71767-111 — furosemide, 71872-7059 — 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.