Furosemide

NDC 72789-032 · PD-Rx Pharmaceuticals, Inc.

Generic namefurosemide

Dosage formTABLET

RouteORAL

Active ingredient(s)FUROSEMIDE

Strength40 mg/1

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

Marketing categoryANDA

Packages

72789-032-30 — 30 TABLET in 1 BOTTLE, PLASTIC (72789-032-30)

72789-032-60 — 60 TABLET in 1 BOTTLE, PLASTIC (72789-032-60)

FDA lists these products with the same active ingredient.

71872-7380 — FUROSEMIDE, 72162-1360 — furosemide, 72162-1361 — furosemide, 72162-1362 — furosemide, 72572-190 — furosemide, 72572-275 — Furosemide, 72603-133 — Furosemide, 72603-251 — Furosemide, 72603-474 — Furosemide, 72789-030 — 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, +194 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.