# Enoxaparin Sodium

NDC: 71288-433
Generic name: Enoxaparin Sodium
Labeler / Manufacturer: Meitheal Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: SUBCUTANEOUS
Marketing started: 20191201

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:"71288-433"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-433
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b6fb85ab-1fe5-4dd3-a97f-adbed0674f67