NDC 70752-294
Mycophenolate Mofetil 200 mg per 1 mL powder, for suspension
On the label: Quagen Pharmaceuticals LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lannett Company, LLC | Seymour, IN, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 21, 2022 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Mycophenolic Acid: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 200 mg per 1 mL
- Approval
- ANDA ANDA214525
- On the market since
- Aug 6, 2026
- Package NDCs
70752-294-60- Official label
- DailyMed (National Library of Medicine), updated Aug 6, 2026
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