# Dextrose

NDC: 0409-6648
Generic name: DEXTROSE MONOHYDRATE
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20050331

FDA application: NDA019445

## Active ingredients

- DEXTROSE MONOHYDRATE: 25 g/50mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-6648"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-6648
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4ed365da-4e62-4329-c1b9-c197ab4fb6e1