NDC 51662-1695
Methylprednisolone Sodium Succinate 125 mg per 2 mL injection
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst 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 |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Methylprednisolone: every company that makes it
- Form
- injection, intravascular; intravenous
- Strength
- 125 mg per 2 mL
- Approval
- ANDA ANDA212396
- On the market since
- Mar 24, 2022
- Package NDCs
51662-1695-151662-1695-251662-1695-3- Official label
- DailyMed (National Library of Medicine), updated Jul 24, 2026
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