FDA NDC Directory · JSON-LD · Markdown

Sertraline Hydrochloride

NDC 64980-409 · HUMAN PRESCRIPTION DRUG · SOLUTION, CONCENTRATE

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078861
Dosage form / routeSOLUTION, CONCENTRATE · ORAL
Active ingredientsSERTRALINE HYDROCHLORIDE (20 mg/mL)
Marketing started20081031
Package count1

External sources

Source: openFDA. Public-domain (CC0).