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ETHACRYNATE SODIUM

NDC 69315-701 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerLeading Pharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208663
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsETHACRYNATE SODIUM (50 mg/50mL)
Marketing started20260109
Package count1

External sources

Source: openFDA. Public-domain (CC0).