FDA NDC Directory · JSON-LD · Markdown

OXYCODONE HYDROCHLORIDE

NDC 0121-0827 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerPAI Holdings, LLC dba PAI Pharma
Marketing categoryAbbreviated NDA (generic) · App ANDA206914
Dosage form / routeSOLUTION · ORAL
Active ingredientsOXYCODONE HYDROCHLORIDE (5 mg/5mL)
Marketing started20190408
Package count2

External sources

Source: openFDA. Public-domain (CC0).