# ETHACRYNATE SODIUM

NDC: 69315-701
Generic name: ETHACRYNATE SODIUM
Labeler / Manufacturer: Leading Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20260109

FDA application: ANDA208663

## Active ingredients

- ETHACRYNATE SODIUM: 50 mg/50mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69315-701"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69315-701
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e24e7440-a958-6fd0-6bfe-1bd29e638657