NDC 0409-3150
Heparin Sodium 5000 [USP'U] per 100 mL injection, solution
On the label: Hospira, Inc..
Where it's made
This label doesn't name the factory that makes the drug (it lists 1 site that tests it). Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Hospira, Inc. names for other drugs.
Product details
- Generic drug
- Heparin: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 5000 [USP'U] per 100 mL
- Approval
- NDA NDA018916
- On the market since
- Jan 3, 2023
- Package NDCs
0409-3150-050409-3150-20- Official label
- DailyMed (National Library of Medicine), updated May 12, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?