# ETHACRYNATE SODIUM

NDC: 42023-157
Generic name: ethacrynate sodium
Labeler / Manufacturer: Par Health USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20150730

FDA application: ANDA205473

## 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:"42023-157"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42023-157
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3313ed5d-7991-408f-872b-d5a701aa6d83