NDC 70121-1001
Methylprednisolone Sodium Succinate 125 mg per 2 mL injection, powder, lyophilized, for solution
On the label: Amneal Pharmaceuticals LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Amneal Pharmaceuticals Private Limited | Ahmedabad, India | Makes it, tests it, packages it and sterilizes it | No problems foundJun 19, 2024 · 7 inspections |
Product details
- Generic drug
- Methylprednisolone: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intramuscular; intravenous
- Strength
- 125 mg per 2 mL
- Approval
- ANDA ANDA207549
- On the market since
- Nov 11, 2016
- Package NDCs
70121-1001-170121-1001-5- Official label
- DailyMed (National Library of Medicine), updated Dec 15, 2025
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