FDA NDC
voriconazole
This name is from the loaded FDA file.
Source: FDA NDC Directory, live from openFDA. Publisher page
- NDC
- 70436-029
- Proprietary name
- voriconazole
- Nonproprietary name
- voriconazole
- Labeler
- Slate Run Pharmaceuticals
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Strength
- 200 mg/1
HCPCS A9585 Billable units per 11-digit NDC: 1000.
Run it in Rivvi
Which 2027 plans near you dropped or restricted voriconazole?
Tier changes and new prior auth, step therapy or quantity limits, plan by plan, from the CMS Part D files.
Free to start. Opens Rivvi, the AI workspace for healthcare teams.