FDA NDC Directory · JSON-LD · Markdown

Paliperidone

NDC 60687-459 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA205618
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPALIPERIDONE (3 mg/1)
Marketing started20200115
Package count1

External sources

Source: openFDA. Public-domain (CC0).