NDC 55150-210
Bivalirudin 250 mg injection, powder, lyophilized, for solution
On the label: AuroMedics Pharma LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
Product details
- Generic drug
- Bivalirudin: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 250 mg
- Approval
- ANDA ANDA205962
- On the market since
- Jul 27, 2018
- Package NDCs
55150-210-10- Official label
- DailyMed (National Library of Medicine), updated Jul 10, 2026
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