FDA NDC Directory · JSON-LD · Markdown

Sertraline

NDC 50268-770 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAvPAK
Marketing categoryAbbreviated NDA (generic) · App ANDA077670
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSERTRALINE HYDROCHLORIDE (100 mg/1)
Marketing started20240206
Package count1

External sources

Source: openFDA. Public-domain (CC0).