# Heparin Sodium

NDC: 0069-0043
Generic name: Heparin Sodium
Labeler / Manufacturer: Pfizer Laboratories Div Pfizer Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20110721

FDA application: NDA201370

## 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:"0069-0043"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0069-0043
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=56dc3074-f1c5-45a3-b923-f1d14858e06d