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Sertraline Hydrochloride

NDC 55700-362 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerQuality Care Products LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077206
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSERTRALINE HYDROCHLORIDE (100 mg/1)
Marketing started20070206
Marketing ended20270131
Package count1

External sources

Source: openFDA. Public-domain (CC0).