# Dextrose

NDC: 0338-0208
Generic name: Dextrose Monohydrate
Labeler / Manufacturer: Baxter Healthcare Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 19921207

FDA application: NDA020179

## Active ingredients

- DEXTROSE MONOHYDRATE: 5 g/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0338-0208"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0338-0208
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=50603082-bce5-49eb-9737-e04239cfb695