# voriconazole

NDC: 43386-089
Generic name: voriconazole
Labeler / Manufacturer: Lupin Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160524

FDA application: ANDA207371

## Active ingredients

- VORICONAZOLE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43386-089"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43386-089
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b4c934c0-c1bb-4b0a-bc32-fb9e77ef65fc