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Sertraline Hydrochloride

NDC 68180-352 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077670
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSERTRALINE HYDROCHLORIDE (50 mg/1)
Marketing started20070206
Package count4

External sources

Source: openFDA. Public-domain (CC0).