NDC 55154-2380
Heparin Sodium 10000 [USP'U] per 1 mL injection, solution
On the label: Cardinal Health 107, LLC. It's repackaged: Cardinal Health 107, LLC rebottles it from Hospira, Inc.'s NDC 0409-1316.
Where the pills inside were 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
- Dec 7, 2009
- Package NDCs
55154-2380-5- Official label
- DailyMed (National Library of Medicine), updated Jul 10, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?