# Voriconazole

NDC: 72843-441
Generic name: voriconazole
Labeler / Manufacturer: UBI Pharma Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20200831

FDA application: ANDA211264

## 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:"72843-441"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72843-441
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9a81e485-7f26-45b6-bfd7-6114afb7def9