NDC 51662-1486
Heparin Sodium 10000 [USP'U] per 1 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 0409-2721.
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 |
| Pfizer Healthcare India Private Limited | Anakapalli, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 18, 2022 · 7 inspections, 1 with FDA action |
| Pharmacia Hepar LLC | Franklin, OH, United States | Makes the active ingredient and tests it | No problems foundMay 1, 2024 · 12 inspections |
| Hospira, Inc. | McPherson, KS, United States | Tests it | Problems found, fixed voluntarilyJan 17, 2025 · 16 inspections, 2 with FDA action |
| Pharmacia & Upjohn Company LLC | Kalamazoo, MI, United States | Tests it | Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections |
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; subcutaneous
- Strength
- 10000 [USP'U] per 1 mL
- Approval
- ANDA ANDA090571
- On the market since
- Mar 9, 2020
- Package NDCs
51662-1486-1- Official label
- DailyMed (National Library of Medicine), updated May 7, 2025
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