NDC 71839-117
Heparin Sodium 2000 [USP'U] per 2 mL injection, solution
On the label: BE Pharmaceuticals 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
- Heparin: every company that makes it
- Form
- injection, solution, intravenous; subcutaneous
- Strength
- 2000 [USP'U] per 2 mL
- Approval
- ANDA ANDA214804
- On the market since
- Dec 29, 2020
- Package NDCs
71839-117-0171839-117-25- Official label
- DailyMed (National Library of Medicine), updated Oct 30, 2024
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