Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Janssen Biologics B.V. | Leiden, Netherlands | Makes the active ingredient and tests it | Problems found, fixed voluntarilyJun 1, 2023 · 7 inspections |
| Janssen Sciences Ireland UC | CO Cork, Ireland | Makes the active ingredient and tests it | Problems found, fixed voluntarilyJan 12, 2024 · 5 inspections |
| Simtra US LLC | Bloomington, IN, United States | Makes it and tests it | Problems found, fixed voluntarilySep 24, 2024 · 12 inspections |
| AndersonBrecon Inc. | Rockford, IL, United States | Packages it and labels it | No problems foundAug 19, 2026 · 11 inspections |
| Cilag AG | Schaffhausen, Switzerland | Tests it, packages it and labels it | No problems foundNov 21, 2025 · 8 inspections |
Product details
- Generic drug
- Golimumab: every company that makes it
- Form
- injection, solution, subcutaneous
- Strength
- 50 mg per 0.5 mL
- Approval
- BLA BLA125289
- On the market since
- Apr 25, 2009
- Package NDCs
57894-070-0157894-070-0257894-070-8957894-070-90- Official label
- DailyMed (National Library of Medicine), updated Nov 2, 2026
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