# Voriconazole

NDC: 65219-190
Generic name: Voriconazole
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20201201

FDA application: ANDA211099

## Active ingredients

- VORICONAZOLE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-190"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-190
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=25eb8d91-5abd-4fdb-a331-dacc960a95d9