Mannitol

NDC 0409-4031 · Hospira, Inc.

Generic nameMANNITOL

Dosage formINJECTION, SOLUTION

RouteINTRAVENOUS

Active ingredient(s)MANNITOL

Strength12.5 g/50mL

Pharmacologic classIncreased Diuresis [PE], Osmotic Activity [MoA], Osmotic Diuretic [EPC]

Marketing categoryNDA

Packages

0409-4031-01 — 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4031-01) / 50 mL in 1 VIAL, SINGLE-DOSE (0409-4031-16)

J2151 — Injection, mannitol, 250 mg Medicare Part B payment limit (ASP + 6%): $0.07

FDA lists these products with the same active ingredient.

0264-7578 — MANNITOL, 0338-0353 — Mannitol, 0338-0357 — Mannitol, 0404-9905 — Mannitol, 0990-7715 — MANNITOL, 0990-7981 — SORBITOL and MANNITOL, 51662-1468 — MANNITOL, 63323-024 — MANNITOL, 73180-005 — Analgesic, 73180-075 — Analgesic, 84549-024 — MANNITOL

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