NDC 83301-0082
Ganirelix Acetate 250 ug per 0.5 mL injection, solution
On the label: Mullan Pharmaceutical Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Qilu Pharmaceutical Co., Ltd. (Biological Industrial Park) | Jinan, China | Makes it | Problems found, fixed voluntarilyMay 8, 2026 · 1 inspection |
Product details
- Generic drug
- Ganirelix: every company that makes it
- Form
- injection, solution, subcutaneous
- Strength
- 250 ug per 0.5 mL
- Approval
- ANDA ANDA218855
- On the market since
- Jan 13, 2026
- Package NDCs
83301-0082-1- Official label
- DailyMed (National Library of Medicine), updated May 11, 2026
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