Package 60505-4774-3

Brand: vilazodone

Generic: vilazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60505-4774-3
Digits Only 6050547743
Product NDC 60505-4774
Product ID 60505-4774_cc72732d-7d9f-421b-9aff-ffc577aa3e4e
Description

30 TABLET in 1 BOTTLE (60505-4774-3)

Marketing

Marketing Status
Discontinued 2026-04-30
Brand vilazodone
Generic vilazodone hydrochloride
Sample Package No

Linked Drug Pages (1)

vilazodone, Vilazodone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cc72732d-7d9f-421b-9aff-ffc577aa3e4e", "openfda": {"unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["fad37b72-1ebe-4a71-835d-b0c1e4b90011"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (60505-4774-3)", "package_ndc": "60505-4774-3", "marketing_end_date": "20260430", "marketing_start_date": "20220604"}], "brand_name": "Vilazodone", "product_id": "60505-4774_cc72732d-7d9f-421b-9aff-ffc577aa3e4e", "dosage_form": "TABLET", "product_ndc": "60505-4774", "generic_name": "vilazodone hydrochloride", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vilazodone", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "NDA022567", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260430", "marketing_start_date": "20220604"}