# Enoxaparin Sodium

NDC: 70710-1763
Generic name: Enoxaparin Sodium
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20210401

FDA application: ANDA076726

## Active ingredients

- ENOXAPARIN SODIUM: 150 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70710-1763"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1763
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d8afb29f-cbed-43bc-809f-09b30fca28f5