NDC 23155-848
Mycophenolate Mofetil 200 mg per 1 mL powder, for suspension
On the label: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Strides Pharma Science Limited | Bengaluru, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMay 20, 2026 · 11 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 ANDA212634
- On the market since
- Sep 5, 2023
- Package NDCs
23155-848-51- Official label
- DailyMed (National Library of Medicine), updated Dec 26, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?