# enoxaparin sodium

NDC: 71839-112
Generic name: enoxaparin sodium
Labeler / Manufacturer: BE Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: SUBCUTANEOUS
Marketing started: 20230616

FDA application: ANDA214646

## Active ingredients

- ENOXAPARIN SODIUM: 80 mg/.8mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71839-112"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71839-112
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b7197534-1daa-42de-8b83-a727da1195bf