FDA NDC Directory · JSON-LD · Markdown

oxycodone and acetaminophen

NDC 72887-682 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerFH2 Pharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040608
Dosage form / routeTABLET · ORAL
Active ingredientsACETAMINOPHEN (300 mg/1)
OXYCODONE HYDROCHLORIDE (7.5 mg/1)
Marketing started20210302
Package count1

External sources

Source: openFDA. Public-domain (CC0).