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Sertraline Hydrochloride

NDC 87441-075 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerUnit Dose Solutions, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077670
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSERTRALINE HYDROCHLORIDE (25 mg/1)
Marketing started20260706
Package count1

External sources

Source: openFDA. Public-domain (CC0).