FDA NDC Directory · JSON-LD · Markdown

Oxycodone and Acetaminophen

NDC 60687-642 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA207510
Dosage form / routeTABLET · ORAL
Active ingredientsACETAMINOPHEN (325 mg/1)
OXYCODONE HYDROCHLORIDE (5 mg/1)
Marketing started20220104
Package count1

External sources

Source: openFDA. Public-domain (CC0).