NDC 70436-029
voriconazole 200 mg injection, powder, lyophilized, for solution
On the label: Slate Run Pharmaceuticals, LLC..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hainan Poly Pharm. Co., Ltd. | Haikou, China | Makes it | Problems found, fixed voluntarilyJun 30, 2023 · 4 inspections |
Product details
- Generic drug
- Voriconazole: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 200 mg
- Approval
- ANDA ANDA211661
- On the market since
- Jan 28, 2019
- Package NDCs
70436-029-80- Official label
- DailyMed (National Library of Medicine), updated May 7, 2026
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