Package 70518-4483-0

Brand: trintellix

Generic: vortioxetine
NDC Package

Package Facts

Identity

Package NDC 70518-4483-0
Digits Only 7051844830
Product NDC 70518-4483
Product ID 70518-4483_3f8c7339-73cd-5934-e063-6394a90a5d15
Description

30 POUCH in 1 BOX (70518-4483-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4483-1)

Marketing

Marketing Status
Marketed Since 2025-09-24
Brand trintellix
Generic vortioxetine
Sample Package No

Linked Drug Pages (1)

Trintellix ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f8c7339-73cd-5934-e063-6394a90a5d15", "openfda": {"unii": ["TKS641KOAY"], "rxcui": ["1439812", "1790892"], "spl_set_id": ["bd0107e5-1cb9-4b40-a6af-fa65fcbe6b4e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 BOX (70518-4483-0)  / 1 TABLET, FILM COATED in 1 POUCH (70518-4483-1)", "package_ndc": "70518-4483-0", "marketing_start_date": "20250924"}], "brand_name": "Trintellix", "product_id": "70518-4483_3f8c7339-73cd-5934-e063-6394a90a5d15", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-4483", "generic_name": "vortioxetine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trintellix", "active_ingredients": [{"name": "VORTIOXETINE HYDROBROMIDE", "strength": "5 mg/1"}], "application_number": "NDA204447", "marketing_category": "NDA", "marketing_start_date": "20250924", "listing_expiration_date": "20261231"}