Package 0480-2044-56

Brand: vilazodone hydrochloride

Generic: vilazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0480-2044-56
Digits Only 0480204456
Product NDC 0480-2044
Product ID 0480-2044_5e283aac-a23f-4dd5-870e-19ca577b9000
Description

30 TABLET, FILM COATED in 1 BOTTLE (0480-2044-56)

Marketing

Marketing Status
Marketed Since 2022-06-06
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": "5e283aac-a23f-4dd5-870e-19ca577b9000", "openfda": {"unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["3a4745a0-de23-4b40-923e-0d7dfe6b8634"], "manufacturer_name": ["Teva Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0480-2044-56)", "package_ndc": "0480-2044-56", "marketing_start_date": "20220606"}], "brand_name": "Vilazodone Hydrochloride", "product_id": "0480-2044_5e283aac-a23f-4dd5-870e-19ca577b9000", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0480-2044", "generic_name": "Vilazodone Hydrochloride", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vilazodone Hydrochloride", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA208212", "marketing_category": "ANDA", "marketing_start_date": "20220606", "listing_expiration_date": "20261231"}