NDC 51662-1578
Heparin Sodium In Sodium Chloride 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 Fresenius Kabi, LLC's NDC 63323-517.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| HP Halden Pharma AS | Halden, Norway | Makes it, tests it and packages it | Problems found, fixed voluntarilyMay 10, 2023 · 7 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
- Strength
- 10000 [USP'U] per 100 mL
- Approval
- NDA NDA017029
- On the market since
- Jul 15, 2021
- Package NDCs
51662-1578-1- Official label
- DailyMed (National Library of Medicine), updated Jan 27, 2024
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