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Sertraline

NDC 68788-4183 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076465
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSERTRALINE HYDROCHLORIDE (25 mg/1)
Marketing started20260820
Package count4

External sources

Source: openFDA. Public-domain (CC0).