# voriconazole

NDC: 70436-230
Generic name: voriconazole
Labeler / Manufacturer: Slate Run Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20240301

FDA application: ANDA216805

## Active ingredients

- VORICONAZOLE: 40 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70436-230"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70436-230
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2b262849-9a29-44a2-9b9d-2378f771379c