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Sertraline Hydrochloride

NDC 65862-224 · HUMAN PRESCRIPTION DRUG · SOLUTION, CONCENTRATE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078861
Dosage form / routeSOLUTION, CONCENTRATE · ORAL
Active ingredientsSERTRALINE HYDROCHLORIDE (20 mg/mL)
Marketing started20081031
Package count2

External sources

Source: openFDA. Public-domain (CC0).