# Zortress

NDC: 0078-0422
Generic name: everolimus
Labeler / Manufacturer: Novartis Pharmaceuticals Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20100422

FDA application: NDA021560

## Active ingredients

- EVEROLIMUS: 1 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0078-0422"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0078-0422
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e082a024-7850-400b-a5c2-2a140612562a