Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fareva Pau | Idron, France | Makes it and tests it | Problems found, fixed voluntarilyJan 17, 2025 · 10 inspections, 2 with FDA action |
| ScinoPharm Taiwan, Ltd. | Tainan, Taiwan | Makes the active ingredient | Serious problems, FDA actionJun 23, 2026 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Leuprolide: every company that makes it
- Form
- injection, emulsion, subcutaneous
- Strength
- 42 mg per 0.37 g
- Approval
- NDA NDA211488
- On the market since
- May 19, 2025
- Package NDCs
69448-023-63- Official label
- DailyMed (National Library of Medicine), updated Feb 18, 2026
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