NDC 55150-265
Methylprednisolone Sodium Succinate 2 g injection, powder, lyophilized, for solution
On the label: AuroMedics Pharma LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
Product details
- Generic drug
- Methylprednisolone: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intramuscular; intravenous
- Strength
- 2 g
- Approval
- ANDA ANDA207667
- On the market since
- Dec 15, 2015
- Package NDCs
55150-265-50- Official label
- DailyMed (National Library of Medicine), updated Jun 12, 2026
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