FDA NDC Directory · JSON-LD · Markdown

SAPROPTERIN DIHYDROCHLORIDE

NDC 49884-873 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Labeler / ManufacturerPar Health USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210027
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsSAPROPTERIN DIHYDROCHLORIDE (500 mg/1)
Marketing started20201001
Package count1

External sources

Source: openFDA. Public-domain (CC0).