NDC 63323-258
Methylprednisolone Sodium Succinate 125 mg per 2 mL injection, powder, lyophilized, for solution
On the label: Fresenius Kabi, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Melrose Park, IL, United States | Makes it and tests it | Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action |
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 ANDA040583
- On the market since
- Nov 30, 2004
- Package NDCs
63323-258-0163323-258-03- Official label
- DailyMed (National Library of Medicine), updated Mar 2, 2023
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