NDC 72603-751
Mycophenolate Mofetil 200 mg per 1 mL powder, for suspension
On the label: Northstar Rx LLC..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 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 ANDA218227
- On the market since
- Mar 1, 2026
- Package NDCs
72603-751-01- Official label
- DailyMed (National Library of Medicine), updated Jan 8, 2026
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