Package 60505-4373-3

Brand: vilazodone hydrochloride

Generic: vilazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60505-4373-3
Digits Only 6050543733
Product NDC 60505-4373
Product ID 60505-4373_cf01e721-c246-593a-b0f8-20e03347b9a1
Description

30 TABLET in 1 BOTTLE (60505-4373-3)

Marketing

Marketing Status
Marketed Since 2023-10-26
Brand vilazodone hydrochloride
Generic vilazodone hydrochloride
Sample Package No

Linked Drug Pages (1)

vilazodone hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cf01e721-c246-593a-b0f8-20e03347b9a1", "openfda": {"unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["a70fd858-cbef-7336-d7ce-c78499031644"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (60505-4373-3)", "package_ndc": "60505-4373-3", "marketing_start_date": "20231026"}], "brand_name": "vilazodone hydrochloride", "product_id": "60505-4373_cf01e721-c246-593a-b0f8-20e03347b9a1", "dosage_form": "TABLET", "product_ndc": "60505-4373", "generic_name": "vilazodone hydrochloride", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "vilazodone hydrochloride", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA208228", "marketing_category": "ANDA", "marketing_start_date": "20231026", "listing_expiration_date": "20261231"}