FDA NDC Directory · JSON-LD · Markdown

Paroxetine

NDC 0615-8359 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Marketing categoryAbbreviated NDA (generic) · App ANDA078406
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE (10 mg/1)
Marketing started20091203
Package count1

External sources

Source: openFDA. Public-domain (CC0).