FDA NDC Directory · JSON-LD · Markdown

Zoloft

NDC 58151-575 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namesertraline hydrochloride
Labeler / ManufacturerViatris Specialty LLC
Marketing categoryNew Drug Application (innovator) · App NDA019839
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSERTRALINE HYDROCHLORIDE (50 mg/1)
Marketing started20250708
Package count2

External sources

Source: openFDA. Public-domain (CC0).