NDC 70121-1000
Methylprednisolone Sodium Succinate 40 mg per 1 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
- 40 mg per 1 mL
- Approval
- ANDA ANDA207549
- On the market since
- Nov 11, 2016
- Package NDCs
70121-1000-170121-1000-5- Official label
- DailyMed (National Library of Medicine), updated Dec 15, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?