Package 72205-261-30

Brand: vilazodone hydrochloride

Generic: vilazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72205-261-30
Digits Only 7220526130
Product NDC 72205-261
Product ID 72205-261_c3e167cd-7f56-45eb-80df-a60fa1392e57
Description

30 TABLET in 1 BOTTLE (72205-261-30)

Marketing

Marketing Status
Marketed Since 2023-07-14
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": "c3e167cd-7f56-45eb-80df-a60fa1392e57", "openfda": {"upc": ["0372205262300", "0372205261303", "0372205260306"], "unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["c3e167cd-7f56-45eb-80df-a60fa1392e57"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72205-261-30)", "package_ndc": "72205-261-30", "marketing_start_date": "20230714"}], "brand_name": "vilazodone hydrochloride", "product_id": "72205-261_c3e167cd-7f56-45eb-80df-a60fa1392e57", "dosage_form": "TABLET", "product_ndc": "72205-261", "generic_name": "vilazodone hydrochloride", "labeler_name": "Novadoz Pharmaceuticals LLC", "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": "20230707", "listing_expiration_date": "20261231"}