NDC 83270-000
mycophenolate mofetil 500 mg per 20 mL injection, powder, lyophilized, for solution
On the label: Onesource Specialty Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Onesource Specialty Pharma Limited | Bengaluru Rural, India | Makes it and tests it | Problems found, fixed voluntarilyMar 28, 2025 · 1 inspection |
Product details
- Generic drug
- Mycophenolic Acid: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 500 mg per 20 mL
- Approval
- ANDA ANDA216390
- On the market since
- Apr 30, 2023
- Package NDCs
83270-000-04- Official label
- DailyMed (National Library of Medicine), updated Nov 6, 2025
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