NDC 82094-405
Methylprednisolone Sodium Succinate 2 g per 30.6 mL injection, powder, lyophilized, for solution
On the label: Tianjin Kingyork Pharmaceuticals Co., Ltd.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Tianjin Kingyork Pharmaceuticals Co., Ltd. | Tianjin, China | Makes it and tests it | Problems found, fixed voluntarilyJul 26, 2024 · 4 inspections |
Product details
- Generic drug
- Methylprednisolone: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intramuscular; intravenous
- Strength
- 2 g per 30.6 mL
- Approval
- ANDA ANDA212396
- On the market since
- Apr 20, 2021
- Package NDCs
82094-405-0182094-405-50- Official label
- DailyMed (National Library of Medicine), updated Dec 18, 2025
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