FDA NDC Directory · JSON-LD · Markdown

Oxycodone and Acetaminophen

NDC 42858-102 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerRhodes Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA201278
Dosage form / routeTABLET · ORAL
Active ingredientsACETAMINOPHEN (325 mg/1)
OXYCODONE HYDROCHLORIDE (5 mg/1)
Marketing started20140828
Package count3

External sources

Source: openFDA. Public-domain (CC0).