# Heparin Sodium

NDC: 0404-9872
Generic name: Heparin Sodium
Labeler / Manufacturer: Henry Schein, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20220111

FDA application: ANDA090808

## Active ingredients

- HEPARIN SODIUM: 5000 [USP'U]/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0404-9872"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0404-9872
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=45dc6b8b-ed5d-40a2-8d9c-084c863ae93a