NDC 0781-3158
bivalirudin 250 mg injection, powder, lyophilized, for solution
On the label: Sandoz Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Novetide Ltd. | Netanya, Israel | Makes the active ingredient | No problems foundNov 14, 2019 · 3 inspections |
Product details
- Generic drug
- Bivalirudin: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 250 mg
- Approval
- NDA authorized generic NDA020873
- On the market since
- Jun 15, 2015
- Package NDCs
0781-3158-940781-3158-95- Official label
- DailyMed (National Library of Medicine), updated Sep 30, 2019
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