# Enoxaparin Sodium

NDC: 71288-426
Generic name: Enoxaparin Sodium
Labeler / Manufacturer: Meitheal Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20220614

FDA application: ANDA214856

## Active ingredients

- ENOXAPARIN SODIUM: 300 mg/3mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71288-426"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-426
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=adfc2b23-00a5-4f05-a08b-83087e1e4843