NDC 70518-2023
Solu-Medrol 125 mg per 2 mL injection, powder, for solution
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Pharmacia & Upjohn Company LLC's NDC 0009-0047.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Pharmacia & Upjohn Company LLC | Kalamazoo, MI, United States | Makes it, makes the active ingredient, tests it, packages it and labels it | Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections |
Product details
- Generic drug
- Methylprednisolone: every company that makes it
- Form
- injection, powder, for solution, intramuscular; intravenous
- Strength
- 125 mg per 2 mL
- Approval
- NDA NDA011856
- On the market since
- Apr 15, 2019
- Package NDCs
70518-2023-070518-2023-1- Official label
- DailyMed (National Library of Medicine), updated Jan 30, 2026
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