FDA NDC Directory · JSON-LD · Markdown

SERTRALINE HYDROCHLORIDE

NDC 68788-8210 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202825
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSERTRALINE HYDROCHLORIDE (100 mg/1)
Marketing started20220606
Package count3

External sources

Source: openFDA. Public-domain (CC0).