NDC 43598-671
Fosaprepitant 150 mg injection, powder, lyophilized, for solution
On the label: Dr. Reddy's Laboratories Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr.reddy's Laboratories Limited | Visakhapatnam, India | Makes it and tests it | Problems found, fixed voluntarilyMay 17, 2024 · 9 inspections, 2 with FDA action |
Product details
- Generic drug
- Aprepitant: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 150 mg
- Approval
- ANDA ANDA211160
- On the market since
- Feb 12, 2026
- Package NDCs
43598-671-11- Official label
- DailyMed (National Library of Medicine), updated May 22, 2025
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