# Dextrose

NDC: 65219-240
Generic name: Dextrose Monohydrate
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20161021

FDA application: ANDA207449

## Active ingredients

- DEXTROSE MONOHYDRATE: 25000 mg/500mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-240"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-240
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bd250a46-d229-4e80-b5a1-b34169ccecc4