NDC 70436-025
bivalirudin 250 mg injection, powder, lyophilized, for suspension
On the label: Slate Run Pharmaceuticals, LLC..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hainan Poly Pharm. Co., Ltd. | Haikou, China | Makes it | Problems found, fixed voluntarilyJun 30, 2023 · 4 inspections |
Product details
- Generic drug
- Bivalirudin: every company that makes it
- Form
- injection, powder, lyophilized, for suspension, intravenous
- Strength
- 250 mg
- Approval
- ANDA ANDA213078
- On the market since
- Jun 30, 2021
- Package NDCs
70436-025-8070436-025-82- Official label
- DailyMed (National Library of Medicine), updated Jun 9, 2021
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