# voriconazole

NDC: 68462-573
Generic name: voriconazole
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20150904
Marketing ended: 20270101
FDA application: ANDA203503

## 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:"68462-573"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-573
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4cbac6ad-0faa-4181-a830-27a9f1536b7a