FDA NDC Directory · JSON-LD · Markdown

Sertraline Hydrochloride

NDC 70710-1948 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerZydus Pharmaceuticals (USA) Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA220275
Dosage form / routeCAPSULE · ORAL
Active ingredientsSERTRALINE HYDROCHLORIDE (150 mg/1)
Marketing started20260129
Package count1

External sources

Source: openFDA. Public-domain (CC0).