NDC 16571-282
Mycophenolate Mofetil 200 mg per 1 mL powder, for suspension
On the label: Rising Pharma Holdings, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Corerx, Inc. | Clearwater, FL, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyFeb 26, 2026 · 5 inspections |
Product details
- Generic drug
- Mycophenolic Acid: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 200 mg per 1 mL
- Approval
- ANDA ANDA213955
- On the market since
- Oct 15, 2026
- Package NDCs
16571-282-17- Official label
- DailyMed (National Library of Medicine), updated Oct 13, 2026
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