NDC 63323-118
Heparin Sodium 5000 [USP'U] per 0.5 mL injection, solution
On the label: Fresenius Kabi, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Wilson, NC, United States | Makes it and tests it | Problems found, fixed voluntarilyFeb 13, 2026 · 5 inspections |
Product details
- Generic drug
- Heparin: every company that makes it
- Form
- injection, solution, intravenous; subcutaneous
- Strength
- 5000 [USP'U] per 0.5 mL
- Approval
- NDA NDA017029
- On the market since
- Nov 16, 2018
- Package NDCs
63323-118-0163323-118-05- Official label
- DailyMed (National Library of Medicine), updated Aug 15, 2025
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