FDA NDC Directory · JSON-LD · Markdown

RoxyBond

NDC 81140-101 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Generic nameOxycodone hydrochloride
Labeler / ManufacturerProtega Pharmaceuticals Inc
Marketing categoryNew Drug Application (innovator) · App NDA209777
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsOXYCODONE HYDROCHLORIDE (5 mg/1)
Marketing started20170420
Package count1

External sources

Source: openFDA. Public-domain (CC0).