# Enoxaparin Sodium

NDC: 0781-3262
Generic name: Enoxaparin Sodium
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: SUBCUTANEOUS
Marketing started: 20100723

FDA application: ANDA077857

## Active ingredients

- ENOXAPARIN SODIUM: 100 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-3262"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-3262
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=38f60bd8-b518-4098-a808-b8f5a3ae6a3a