# Enoxaparin Sodium

NDC: 0548-5604
Generic name: Enoxaparin sodium
Labeler / Manufacturer: Amphastar Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: SUBCUTANEOUS
Marketing started: 20110919

FDA application: ANDA076684

## 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:"0548-5604"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0548-5604
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3e6bf2b3-9339-4104-bda3-ad86a1949703