NDC 0409-4031

Mannitol 12.5 g per 50 mL injection, solution

On the label: Hospira, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Hospira, Inc.Rocky Mount, NC, United StatesMakes it, tests it, packages it and labels it No problems foundFeb 7, 2025 · 11 inspections, 3 with FDA action

Product details

Generic drug
Mannitol: every company that makes it
Form
injection, solution, intravenous
Strength
12.5 g per 50 mL
Approval
NDA NDA016269
On the market since
Nov 30, 2004
Package NDCs
0409-4031-01 0409-4031-16
Official label
DailyMed (National Library of Medicine), updated Apr 21, 2026

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