NDC 69097-830
fosaprepitant 150 mg per 5 mL injection, powder, lyophilized, for solution
On the label: Cipla USA., Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Be Biosol Private Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyNov 12, 2024 · 3 inspections |
Product details
- Generic drug
- Aprepitant: every company that makes it
- Form
- injection, powder, lyophilized, for solution
- Strength
- 150 mg per 5 mL
- Approval
- ANDA ANDA212309
- On the market since
- Sep 5, 2019
- Package NDCs
69097-830-37- Official label
- DailyMed (National Library of Medicine), updated Feb 16, 2021
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