FDA NDC Directory · JSON-LD · Markdown

Oxycodone and Acetaminophen

NDC 49999-852 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerQuality Care products LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA087463
Dosage form / routeTABLET · ORAL
Active ingredientsACETAMINOPHEN (325 mg/1)
OXYCODONE HYDROCHLORIDE (5 mg/1)
Marketing started20100610
Marketing ended20290228
Package count4

External sources

Source: openFDA. Public-domain (CC0).