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Paroxetine

NDC 69117-0027 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerYiling Pharmaceutical, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211248
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE HEMIHYDRATE (40 mg/1)
Marketing started20211102
Package count5

External sources

Source: openFDA. Public-domain (CC0).