# Dextrose

NDC: 70518-4452
Generic name: Dextrose monohydrate
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20250822

FDA application: NDA019445

## Active ingredients

- DEXTROSE MONOHYDRATE: 250 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4452"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4452
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e2638b45-1141-4391-971d-c0dea825e41c