# Heparin Sodium

NDC: 0641-0391
Generic name: Heparin Sodium
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 19720322

FDA application: NDA017037

## 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:"0641-0391"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0641-0391
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7014808d-cec9-4b2c-8eb5-940493e356ab