# Heparin Sodium

NDC: 71288-449
Generic name: Heparin Sodium
Labeler / Manufacturer: Meitheal Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20250702

FDA application: ANDA211007

## 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:"71288-449"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-449
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=02fb700d-a28c-4d45-b78d-382dc0d5986c