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Paliperidone

NDC 72819-158 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namepaliperidone
Labeler / ManufacturerArchis Pharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203802
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsPALIPERIDONE (3 mg/1)
Marketing started20220427
Package count1

External sources

Source: openFDA. Public-domain (CC0).