# Heparin Sodium

NDC: 63323-047
Generic name: HEPARIN SODIUM
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 19780210

FDA application: NDA017651

## 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:"63323-047"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-047
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d55b4a63-0c04-4874-b74f-9e9b9e8b008c