Package 68788-8734-3

Brand: vilazodone hydrochloride

Generic: vilazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8734-3
Digits Only 6878887343
Product NDC 68788-8734
Product ID 68788-8734_87fcca39-c5dc-4018-9701-c73bff8d42d6
Description

30 TABLET in 1 BOTTLE (68788-8734-3)

Marketing

Marketing Status
Marketed Since 2024-09-16
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": "87fcca39-c5dc-4018-9701-c73bff8d42d6", "openfda": {"unii": ["U8HTX2GK8J"], "rxcui": ["1086778", "1086784"], "spl_set_id": ["061efdcc-40ea-4647-8cc8-01cd1ccca68b"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8734-3)", "package_ndc": "68788-8734-3", "marketing_start_date": "20240916"}], "brand_name": "vilazodone hydrochloride", "product_id": "68788-8734_87fcca39-c5dc-4018-9701-c73bff8d42d6", "dosage_form": "TABLET", "product_ndc": "68788-8734", "generic_name": "vilazodone hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20240916", "listing_expiration_date": "20261231"}