# Dextrose

NDC: 0990-7935
Generic name: dextrose
Labeler / Manufacturer: ICU Medical Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20191001

FDA application: NDA018564

## Active ingredients

- DEXTROSE MONOHYDRATE: 20 g/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0990-7935"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0990-7935
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b5cb7a5a-bbe8-4217-a82e-da818f7771c9