Package 42291-950-30

Brand: vilazodone

Generic: vilazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42291-950-30
Digits Only 4229195030
Product NDC 42291-950
Description

30 TABLET in 1 BOTTLE (42291-950-30)

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48c0f93c-c1dc-21ec-e063-6394a90a357a", "openfda": {"upc": ["0342291950306", "0342291948303"], "unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["1a26f764-1a89-2524-e063-6394a90a28d3"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (42291-950-30)", "package_ndc": "42291-950-30", "marketing_end_date": "20260430", "marketing_start_date": "20240605"}], "brand_name": "Vilazodone", "product_id": "42291-950_48c0f93c-c1dc-21ec-e063-6394a90a357a", "dosage_form": "TABLET", "product_ndc": "42291-950", "generic_name": "vilazodone hydrochloride", "labeler_name": "AvKARE", "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": "20240605"}