# Heparin Sodium

NDC: 0409-2720
Generic name: HEPARIN SODIUM
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20090831

FDA application: ANDA090571

## Active ingredients

- HEPARIN SODIUM: 1000 [USP'U]/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-2720"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-2720
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6c181d7e-aed2-4975-30ac-d39a94cca7ec