# Heparin Sodium

NDC: 63739-920
Generic name: Heparin Sodium
Labeler / Manufacturer: McKesson Corporation dba SKY Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20140612

FDA application: ANDA202957

## Active ingredients

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

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63739-920"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63739-920
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7f05762a-7527-4796-b21e-68277aec379e