Package 72603-815-01

Brand: vilazodone hydrochloride

Generic: vilazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72603-815-01
Digits Only 7260381501
Product NDC 72603-815
Product ID 72603-815_701c8b84-13ae-4adb-af7a-304bf1f21e3b
Description

30 TABLET in 1 BOTTLE (72603-815-01)

Marketing

Marketing Status
Marketed Since 2025-01-01
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": "701c8b84-13ae-4adb-af7a-304bf1f21e3b", "openfda": {"upc": ["0372603815016", "0372603814019", "0372603813012"], "unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["701c8b84-13ae-4adb-af7a-304bf1f21e3b"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72603-815-01)", "package_ndc": "72603-815-01", "marketing_start_date": "20250101"}], "brand_name": "vilazodone hydrochloride", "product_id": "72603-815_701c8b84-13ae-4adb-af7a-304bf1f21e3b", "dosage_form": "TABLET", "product_ndc": "72603-815", "generic_name": "vilazodone hydrochloride", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "vilazodone hydrochloride", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA208228", "marketing_category": "ANDA", "marketing_start_date": "20230707", "listing_expiration_date": "20261231"}