NDC 51662-1264
Solu-Medrol 40 mg per 1 mL injection, powder, for solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Pharmacia & Upjohn Company LLC's NDC 0009-0039.
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 |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Methylprednisolone: every company that makes it
- Form
- injection, powder, for solution, intramuscular; intravenous
- Strength
- 40 mg per 1 mL
- Approval
- NDA NDA011856
- On the market since
- Sep 2, 2018
- Package NDCs
51662-1264-151662-1264-251662-1264-3- Official label
- DailyMed (National Library of Medicine), updated Feb 22, 2024
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