FDA NDC Directory · JSON-LD · Markdown

Risperidone

NDC 69367-372 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerWestminster Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078707
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRISPERIDONE (3 mg/1)
Marketing started20240909
Package count2

External sources

Source: openFDA. Public-domain (CC0).