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Oxycodone Hydchloride

NDC 35356-839 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerQuality Care Products LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA091393
Dosage form / routeTABLET · ORAL
Active ingredientsOXYCODONE HYDROCHLORIDE (10 mg/1)
Marketing started20111220
Marketing ended20270630
Package count3

External sources

Source: openFDA. Public-domain (CC0).