# Heparin Sodium in Sodium Chloride

NDC: 0264-9872
Generic name: Heparin Sodium in Sodium Chloride
Labeler / Manufacturer: B. Braun Medical Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 19920720

FDA application: NDA019953

## Active ingredients

- HEPARIN SODIUM: 200 [USP'U]/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0264-9872"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0264-9872
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a3041c04-0ea8-4d36-81ce-c5091c906316