FDA NDC Directory · JSON-LD · Markdown

SERTRALINE

NDC 76282-213 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameSertraline
Labeler / ManufacturerExelan Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077397
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSERTRALINE HYDROCHLORIDE (50 mg/1)
Marketing started20120820
Package count6

External sources

Source: openFDA. Public-domain (CC0).