NDC 0069-0505
Ngenla 24 mg per 1.2 mL injection, solution
On the label: Pfizer Laboratories Div Pfizer Inc.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Pfizer Ireland Pharmaceuticals Unlimited Company | Dublin, Ireland | Makes the active ingredient and tests it | Problems found, fixed voluntarilyDec 15, 2023 · 5 inspections |
| Pfizer Manufacturing Belgium NV | Puurs-Sint-Amands, Belgium | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJun 22, 2022 · 5 inspections |
| Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC | Andover, MA, United States | Makes the active ingredient and tests it | Problems found, fixed voluntarilyApr 8, 2026 · 5 inspections |
Product details
- Generic drug
- Somatrogon: every company that makes it
- Form
- injection, solution, subcutaneous
- Strength
- 24 mg per 1.2 mL
- Approval
- BLA BLA761184
- On the market since
- Jul 31, 2023
- Package NDCs
0069-0505-010069-0505-02- Official label
- DailyMed (National Library of Medicine), updated Aug 14, 2026
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