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Tapentadol Hydrochloride

NDC 72205-370 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNovadoz Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA220865
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTAPENTADOL HYDROCHLORIDE (75 mg/1)
Marketing started20260903
Package count1

External sources

Source: openFDA. Public-domain (CC0).