vilazodone
Generic: vilazodone hydrochloride
Labeler: avkareDrug Facts
Product Profile
Brand Name
vilazodone
Generic Name
vilazodone hydrochloride
Labeler
avkare
Dosage Form
TABLET
Routes
Active Ingredients
vilazodone hydrochloride 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
42291-949
Product ID
42291-949_48c0f93c-c1dc-21ec-e063-6394a90a357a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA022567
Marketing Start
2024-06-05
Marketing End
2026-04-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42291949
Hyphenated Format
42291-949
Supplemental Identifiers
RxCUI
UPC
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
vilazodone (source: ndc)
Generic Name
vilazodone hydrochloride (source: ndc)
Application Number
NDA022567 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (42291-949-30)
Packages (1)
Ingredients (1)
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 (42291-949-30)", "package_ndc": "42291-949-30", "marketing_end_date": "20260430", "marketing_start_date": "20240605"}], "brand_name": "Vilazodone", "product_id": "42291-949_48c0f93c-c1dc-21ec-e063-6394a90a357a", "dosage_form": "TABLET", "product_ndc": "42291-949", "generic_name": "vilazodone hydrochloride", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vilazodone", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "NDA022567", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260430", "marketing_start_date": "20240605"}