FDA NDC Directory · JSON-LD · Markdown

Oxycodone and Acetaminophen

NDC 31722-192 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207419
Dosage form / routeTABLET · ORAL
Active ingredientsACETAMINOPHEN (325 mg/1)
OXYCODONE HYDROCHLORIDE (5 mg/1)
Marketing started20170411
Package count2

External sources

Source: openFDA. Public-domain (CC0).