NDC 0009-0016
Solu-Cortef 500 mg per 4 mL injection, powder, for solution
On the label: Pharmacia & Upjohn Company LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Pharmacia & Upjohn Company LLC | Kalamazoo, MI, United States | Makes it, makes the active ingredient, tests it and packages it | Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections |
Product details
- Generic drug
- Hydrocortisone: every company that makes it
- Form
- injection, powder, for solution, intramuscular; intravenous
- Strength
- 500 mg per 4 mL
- Approval
- NDA NDA009866
- On the market since
- Apr 27, 1955
- Package NDCs
0009-0016-12- Official label
- DailyMed (National Library of Medicine), updated Sep 29, 2026
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