# Mannitol

NDC: 0409-4031
Generic name: MANNITOL
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20041130

FDA application: NDA016269

## Active ingredients

- MANNITOL: 12.5 g/50mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-4031"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-4031
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8ad3145e-00e7-4412-b9a5-06f00f264f30