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Sapropterin dihydrochloride

NDC 72603-194 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Labeler / ManufacturerNorthStar RxLLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215420
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsSAPROPTERIN DIHYDROCHLORIDE (500 mg/1)
Marketing started20231201
Package count1

External sources

Source: openFDA. Public-domain (CC0).