NDC 0781-3522
Methylprednisolone Acetate 40 mg per 1 mL injection, suspension
On the label: Sandoz Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Laboratorio Italiano Biochimico Farmaceutico Lisapharma SPA | Erba, Italy | Makes it | Problems found, fixed voluntarilyJan 26, 2024 · 2 inspections |
Product details
- Generic drug
- Methylprednisolone: every company that makes it
- Form
- injection, suspension
- Strength
- 40 mg per 1 mL
- Approval
- ANDA ANDA214870
- On the market since
- Mar 14, 2024
- Package NDCs
0781-3522-700781-3522-75- Official label
- DailyMed (National Library of Medicine), updated Jul 22, 2024
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