vilazodone hydrochloride
Generic: vilazodone hydrochloride
Labeler: golden state medical supply, inc.Drug Facts
Product Profile
Brand Name
vilazodone hydrochloride
Generic Name
vilazodone hydrochloride
Labeler
golden state medical supply, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
vilazodone hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51407-915
Product ID
51407-915_3b8c8c08-ce7c-b237-e063-6294a90aeb14
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208212
Listing Expiration
2026-12-31
Marketing Start
2019-09-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51407915
Hyphenated Format
51407-915
Supplemental Identifiers
RxCUI
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 hydrochloride (source: ndc)
Generic Name
vilazodone hydrochloride (source: ndc)
Application Number
ANDA208212 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (51407-915-30)
Packages (1)
Ingredients (1)
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 (51407-915-30)", "package_ndc": "51407-915-30", "marketing_start_date": "20250527"}], "brand_name": "Vilazodone Hydrochloride", "product_id": "51407-915_3b8c8c08-ce7c-b237-e063-6294a90aeb14", "dosage_form": "TABLET, FILM COATED", "product_ndc": "51407-915", "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": "10 mg/1"}], "application_number": "ANDA208212", "marketing_category": "ANDA", "marketing_start_date": "20190930", "listing_expiration_date": "20261231"}