# Enoxaparin Sodium

NDC: 68001-636
Generic name: Enoxaparin Sodium
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: SUBCUTANEOUS
Marketing started: 20250115

FDA application: ANDA206834

## 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:"68001-636"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-636
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a2a8615b-a27e-4ab2-ae4c-592bbf4643c0