Package 51407-916-30
Brand: vilazodone hydrochloride
Generic: vilazodone hydrochloridePackage Facts
Identity
Package NDC
51407-916-30
Digits Only
5140791630
Product NDC
51407-916
Description
30 TABLET, FILM COATED in 1 BOTTLE (51407-916-30)
Marketing
Marketing Status
Brand
vilazodone hydrochloride
Generic
vilazodone hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3b8c8c08-ce7c-b237-e063-6294a90aeb14", "openfda": {"unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["3b8ca479-72e9-2431-e063-6394a90af7ff"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (51407-916-30)", "package_ndc": "51407-916-30", "marketing_start_date": "20250527"}], "brand_name": "Vilazodone Hydrochloride", "product_id": "51407-916_3b8c8c08-ce7c-b237-e063-6294a90aeb14", "dosage_form": "TABLET, FILM COATED", "product_ndc": "51407-916", "generic_name": "Vilazodone Hydrochloride", "labeler_name": "Golden State Medical Supply, 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": "20190930", "listing_expiration_date": "20261231"}