# MANNITOL

NDC: 51662-1468
Generic name: MANNITOL
Labeler / Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20191213

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:"51662-1468"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1468
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=999ce711-2d5b-0d7d-e053-2995a90a2689