NDC 63323-262
Heparin Sodium 5000 [USP'U] per 1 mL injection, solution
On the label: Fresenius Kabi, LLC.
Where it's 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 |
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
- 5000 [USP'U] per 1 mL
- Approval
- NDA NDA017029
- On the market since
- Mar 25, 2020
- Package NDCs
63323-262-0363323-262-06- Official label
- DailyMed (National Library of Medicine), updated Apr 30, 2026
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