Package 70518-4284-0

Brand: trintellix

Generic: vortioxetine
NDC Package

Package Facts

Identity

Package NDC 70518-4284-0
Digits Only 7051842840
Product NDC 70518-4284
Product ID 70518-4284_401adb5f-9271-ba24-e063-6294a90a5a84
Description

30 POUCH in 1 BOX (70518-4284-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4284-1)

Marketing

Marketing Status
Marketed Since 2025-02-11
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": "401adb5f-9271-ba24-e063-6294a90a5a84", "openfda": {"unii": ["TKS641KOAY"], "rxcui": ["1439808", "1790886"], "spl_set_id": ["239215eb-be32-4286-9677-1e5556c6cccf"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 BOX (70518-4284-0)  / 1 TABLET, FILM COATED in 1 POUCH (70518-4284-1)", "package_ndc": "70518-4284-0", "marketing_start_date": "20250211"}], "brand_name": "Trintellix", "product_id": "70518-4284_401adb5f-9271-ba24-e063-6294a90a5a84", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-4284", "generic_name": "vortioxetine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trintellix", "active_ingredients": [{"name": "VORTIOXETINE HYDROBROMIDE", "strength": "10 mg/1"}], "application_number": "NDA204447", "marketing_category": "NDA", "marketing_start_date": "20250211", "listing_expiration_date": "20261231"}