NDC 0409-1316
Heparin Sodium 10000 [USP'U] per 1 mL injection, solution
On the label: Hospira, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | McPherson, KS, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJan 17, 2025 · 16 inspections, 2 with FDA action |
| Hospira, Inc. | Rocky Mount, NC, United States | Tests it | No problems foundFeb 7, 2025 · 11 inspections, 3 with FDA action |
Product details
- Generic drug
- Heparin: every company that makes it
- Form
- injection, solution, intravenous; subcutaneous
- Strength
- 10000 [USP'U] per 1 mL
- Approval
- ANDA ANDA089522
- On the market since
- Mar 31, 2005
- Package NDCs
0409-1316-110409-1316-32- Official label
- DailyMed (National Library of Medicine), updated Aug 25, 2026
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