FDA NDC Directory · JSON-LD · Markdown

Zoloft

NDC 0049-4910 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namesertraline hydrochloride
Labeler / ManufacturerROERIG
Marketing categoryNew Drug Application (innovator) · App NDA019839
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSERTRALINE HYDROCHLORIDE (100 mg/1)
Marketing started19920211
Marketing ended20260630
Package count2

External sources

Source: openFDA. Public-domain (CC0).