NDC 0409-7794
Heparin Sodium and Dextrose 5000 [USP'U] per 100 mL injection, solution
On the label: Hospira, Inc..
Where it's 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 |
| Hospira, Inc. | McPherson, KS, United States | Tests it | Problems found, fixed voluntarilyJan 17, 2025 · 16 inspections, 2 with FDA action |
Recalls
- Jun 6, 2014 · Class II · Hospira Inc.
Lack of Assurance of Sterility: Confirmed consumer report of fluid leaking from primary container of bag.
Lots: Lot # 34-811-KL, 36-106-KL, 36-114-KL; Exp. 12/15; 36-101-KL, Exp. 12/15; 37-202-KL, Exp. 1/16; 38-302-KL, Exp. 2/16; 38-305-KL, Exp. 2/16
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
- Strength
- 5000 [USP'U] per 100 mL
- Approval
- NDA NDA019339
- On the market since
- Jun 13, 2006
- Package NDCs
0409-7794-520409-7794-62- Official label
- DailyMed (National Library of Medicine), updated May 25, 2026
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