# Voriconazole

NDC: 70594-067
Generic name: Voriconazole
Labeler / Manufacturer: Xellia Pharmaceuticals USA LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20230824

FDA application: NDA208562

## Active ingredients

- VORICONAZOLE: 10 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70594-067"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70594-067
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9ec6eda2-2f15-423b-9ec6-819379a426e1