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Sertraline Hydrochloride

NDC 84386-099 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA077206
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSERTRALINE HYDROCHLORIDE (100 mg/1)
Marketing started20251120
Package count8

External sources

Source: openFDA. Public-domain (CC0).