vilazodone hydrochloride

Generic: vilazodone hydrochloride

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

Drug Facts

Product Profile

Brand Name vilazodone hydrochloride
Generic Name vilazodone hydrochloride
Labeler teva pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

vilazodone hydrochloride 40 mg/1

Manufacturer
Teva Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 0480-2043
Product ID 0480-2043_5e283aac-a23f-4dd5-870e-19ca577b9000
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208212
Listing Expiration 2026-12-31
Marketing Start 2022-06-06

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04802043
Hyphenated Format 0480-2043

Supplemental Identifiers

RxCUI
1086772 1086778 1086784
UNII
U8HTX2GK8J

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (0480-2043-56)
source: ndc

Packages (1)

0480-2043-56 30 TABLET, FILM COATED in 1 BOTTLE (0480-2043-56)

Ingredients (1)

vilazodone hydrochloride (40 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": "5e283aac-a23f-4dd5-870e-19ca577b9000", "openfda": {"unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["3a4745a0-de23-4b40-923e-0d7dfe6b8634"], "manufacturer_name": ["Teva Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0480-2043-56)", "package_ndc": "0480-2043-56", "marketing_start_date": "20220606"}], "brand_name": "Vilazodone Hydrochloride", "product_id": "0480-2043_5e283aac-a23f-4dd5-870e-19ca577b9000", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0480-2043", "generic_name": "Vilazodone Hydrochloride", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vilazodone Hydrochloride", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA208212", "marketing_category": "ANDA", "marketing_start_date": "20220606", "listing_expiration_date": "20261231"}