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Oxycodone and Acetaminophen

NDC 70010-667 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerGranules Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211708
Dosage form / routeTABLET · ORAL
Active ingredientsACETAMINOPHEN (325 mg/1)
OXYCODONE HYDROCHLORIDE (2.5 mg/1)
Marketing started20220101
Package count2

External sources

Source: openFDA. Public-domain (CC0).