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PAROXETINE

NDC 70518-1460 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameparoxetine hydrochloride
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA075356
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE ANHYDROUS (30 mg/1)
Marketing started20181004
Package count1

External sources

Source: openFDA. Public-domain (CC0).