# Osmitrol

NDC: 0338-0353
Generic name: Mannitol
Labeler / Manufacturer: Baxter Healthcare Company
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 19640608

FDA application: NDA013684

## Active ingredients

- MANNITOL: 10 g/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0338-0353"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0338-0353
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0d914965-7001-45cb-ba51-d7c5964b05bc