NDC 51662-1434
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 McKesson Packaging Services Business Unit of McKesson Corporation's NDC 63739-964.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it and tests it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
| Shenzhen Hepalink Pharmaceutical Group Co., Ltd. | Shenzhen, China | Makes the active ingredient | Problems found, fixed voluntarilyJun 13, 2025 · 1 inspection |
| Shenzhen Techdow Pharmaceutical Co., Ltd. | Shenzhen, China | Makes it and tests it | Problems found, fixed voluntarilySep 17, 2019 · 3 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 ANDA203198
- On the market since
- Jan 10, 2020
- Package NDCs
51662-1434-1- Official label
- DailyMed (National Library of Medicine), updated Jan 8, 2025
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