NDC 71288-554
Ganirelix Acetate 250 ug per 0.5 mL injection, solution
On the label: Meitheal Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd (API and FDF Site) | Nanjing, China | Makes it | Problems found, fixed voluntarilyNov 10, 2023 · 3 inspections |
Product details
- Generic drug
- Ganirelix: every company that makes it
- Form
- injection, solution, subcutaneous
- Strength
- 250 ug per 0.5 mL
- Approval
- ANDA ANDA214996
- On the market since
- Jun 6, 2022
- Package NDCs
71288-554-80- Official label
- DailyMed (National Library of Medicine), updated Feb 20, 2025
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