vilazodone hydrochloride

Generic: vilazodone hydrochloride

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vilazodone hydrochloride
Generic Name vilazodone hydrochloride
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

vilazodone hydrochloride 20 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8734
Product ID 68788-8734_87fcca39-c5dc-4018-9701-c73bff8d42d6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208228
Listing Expiration 2026-12-31
Marketing Start 2024-09-16

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888734
Hyphenated Format 68788-8734

Supplemental Identifiers

RxCUI
1086778 1086784
UNII
U8HTX2GK8J

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 ANDA208228 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68788-8734-3)
source: ndc

Packages (1)

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

Ingredients (1)

vilazodone hydrochloride (20 mg/1)

Linked Drug Pages (1)

vilazodone hydrochloride ndc-match (0.9)

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"}