FDA NDC Directory · JSON-LD · Markdown

Sertraline Hydrochloride

NDC 70954-899 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA219714
Dosage form / routeCAPSULE · ORAL
Active ingredientsSERTRALINE HYDROCHLORIDE (150 mg/1)
Marketing started20260120
Package count1

External sources

Source: openFDA. Public-domain (CC0).