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Oxycodone and Acetaminophen

NDC 71205-329 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA207419
Dosage form / routeTABLET · ORAL
Active ingredientsACETAMINOPHEN (325 mg/1)
OXYCODONE HYDROCHLORIDE (5 mg/1)
Marketing started20170411
Package count5

External sources

Source: openFDA. Public-domain (CC0).