NDC 51662-1687
Heparin Sodium 10000 [USP'U] per 100 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Hospira, Inc.'s NDC 0409-7650.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | Rocky Mount, NC, United States | Makes it, tests it, packages it and labels it | No problems foundFeb 7, 2025 · 11 inspections, 3 with FDA action |
| Hospira, Inc. | McPherson, KS, United States | Tests it | Problems found, fixed voluntarilyJan 17, 2025 · 16 inspections, 2 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Heparin: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 10000 [USP'U] per 100 mL
- Approval
- NDA NDA018916
- On the market since
- Jun 30, 2005
- Package NDCs
51662-1687-151662-1687-251662-1687-3- Official label
- DailyMed (National Library of Medicine), updated May 5, 2026
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