Fresenius Kabi USA, LLC
Grand Island, NY, United States · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Oct 13, 2023. 14 inspections on record, 2 with serious problems.
NDC 84549-024
Mannitol 250 mg per 1 mL injection, solution
On the label: ProPharma Distribution.
It's a repackaged product: ProPharma Distribution rebottles it from Fresenius Kabi, LLC's NDC 63323-024.
Where the pills inside were made
Repackaging site
- ProPharma Distribution, Westminster, CO, United States · repackages it and relabels it
Product details
- Generic drug
- Mannitol: see every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 250 mg per 1 mL
- Approval
- ANDA ANDA080677
- On the market since
- Mar 19, 2000
- Package NDCs
84549-024-25- Official label
- DailyMed (National Library of Medicine), updated Nov 7, 2025
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