Furosemide

NDC 71288-203 · Meitheal Pharmaceuticals Inc.

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic nameFurosemide

Dosage formINJECTION, SOLUTION

RouteINTRAMUSCULAR, INTRAVENOUS

Active ingredient(s)FUROSEMIDE

Strength10 mg/mL

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

Marketing categoryANDA

Packages

71288-203-92 — 25 VIAL, SINGLE-DOSE in 1 CARTON (71288-203-92) / 2 mL in 1 VIAL, SINGLE-DOSE (71288-203-91)

71288-203-94 — 25 VIAL, SINGLE-DOSE in 1 CARTON (71288-203-94) / 10 mL in 1 VIAL, SINGLE-DOSE (71288-203-93)

71288-203-03 — 25 VIAL, SINGLE-DOSE in 1 CARTON (71288-203-03) / 2 mL in 1 VIAL, SINGLE-DOSE (71288-203-02)

71288-203-05 — 25 VIAL, SINGLE-DOSE in 1 CARTON (71288-203-05) / 4 mL in 1 VIAL, SINGLE-DOSE (71288-203-04)

71288-203-11 — 25 VIAL, SINGLE-DOSE in 1 CARTON (71288-203-11) / 10 mL in 1 VIAL, SINGLE-DOSE (71288-203-10)

J1938 — Injection, furosemide, 1 mg Medicare Part B payment limit (ASP + 6%): $0.02

FDA lists these products with the same active ingredient.

70518-0251 — Furosemide, 70518-2528 — Furosemide, 70518-3061 — furosemide, 70518-3757 — Furosemide, 70518-4444 — furosemide, 70518-4609 — furosemide, 70518-4679 — Furosemide, 70756-618 — furosemide, 70756-619 — furosemide, 70756-620 — furosemide, 71335-0384 — Furosemide, 71335-0842 — furosemide, 71335-0852 — furosemide, 71335-2317 — Furosemide, 71335-2319 — Furosemide, 71610-049 — furosemide, 71610-096 — furosemide, 71610-634 — furosemide, 71610-635 — furosemide, 71610-636 — 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.