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SERTRALINE HYDROCHLORIDE

NDC 50228-468 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerScieGen Pharmaceuticals Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA076442
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSERTRALINE HYDROCHLORIDE (50 mg/1)
Marketing started20230508
Package count3

External sources

Source: openFDA. Public-domain (CC0).