FDA NDC Directory · JSON-LD · Markdown

Zoloft

NDC 0049-0050 · HUMAN PRESCRIPTION DRUG · SOLUTION, CONCENTRATE

Generic namesertraline hydrochloride
Labeler / ManufacturerROERIG
Marketing categoryNew Drug Application (innovator) · App NDA020990
Dosage form / routeSOLUTION, CONCENTRATE · ORAL
Active ingredientsSERTRALINE HYDROCHLORIDE (20 mg/mL)
Marketing started20170106
Marketing ended20260630
Package count1

External sources

Source: openFDA. Public-domain (CC0).