NDC 51662-1409
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 Fresenius Kabi, LLC's NDC 63323-542.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Grand Island, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyOct 13, 2023 · 14 inspections, 2 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Recalls
- Jan 22, 2014 · Class II · Fresenius Kabi USA, LLC
Subpotent; 18 month time point
Lots: Lot Number: 6004137, Expiration date: 06/2014
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Heparin: every company that makes it
- Form
- injection, solution, intravenous; subcutaneous
- Strength
- 10000 [USP'U] per 1 mL
- Approval
- NDA NDA017029
- On the market since
- Nov 11, 2019
- Package NDCs
51662-1409-151662-1409-251662-1409-3- Official label
- DailyMed (National Library of Medicine), updated Jan 29, 2024
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