NDC 0548-5001
Ganirelix Acetate 250 ug per 0.5 mL injection
On the label: Amphastar Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Amphastar Pharmaceuticals, Inc. | Rancho Cucamonga, CA, United States | Makes it and tests it | Problems found, fixed voluntarilyNov 7, 2025 · 18 inspections |
Product details
- Generic drug
- Ganirelix: every company that makes it
- Form
- injection, subcutaneous
- Strength
- 250 ug per 0.5 mL
- Approval
- ANDA ANDA212613
- On the market since
- Jun 20, 2022
- Package NDCs
0548-5001-00- Official label
- DailyMed (National Library of Medicine), updated Apr 19, 2022
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