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NDC 84549-003 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic namedantrolene sodium
Labeler / ManufacturerProPharma Distribution
Marketing categoryAbbreviated NDA (generic) · App ANDA078378
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsDANTROLENE SODIUM (20 mg/60mL)
Marketing started20210409
Package count1

External sources

Source: openFDA. Public-domain (CC0).