NDC 70518-3684
Methylprednisolone sodium succinate 125 mg per 2 mL injection
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Dr. Reddy's Laboratories Inc.'s NDC 43598-129.
Where the pills inside were 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, intramuscular; intravenous
- Strength
- 125 mg per 2 mL
- Approval
- ANDA ANDA212396
- On the market since
- Mar 17, 2023
- Package NDCs
70518-3684-070518-3684-1- Official label
- DailyMed (National Library of Medicine), updated Apr 15, 2026
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