NDC 0404-9872
Heparin Sodium 5000 [USP'U] per 1 mL injection, solution
On the label: Henry Schein, Inc.. It's repackaged: Henry Schein, Inc. rebottles it from Sagent Pharmaceuticals's NDC 25021-402.
Where the pills inside were made
This label doesn't name the factory that makes the drug. 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 Sagent Pharmaceuticals names for other drugs.
Product details
- Generic drug
- Heparin: every company that makes it
- Form
- injection, solution, intravenous; subcutaneous
- Strength
- 5000 [USP'U] per 1 mL
- Approval
- ANDA ANDA090808
- On the market since
- Jan 11, 2022
- Package NDCs
0404-9872-01- Official label
- DailyMed (National Library of Medicine), updated Aug 19, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?