vilazodone

Generic: vilazodone hydrochloride

Labeler: apotex corp
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name vilazodone
Generic Name vilazodone hydrochloride
Labeler apotex corp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

vilazodone hydrochloride 40 mg/1

Manufacturer
Apotex Corp

Identifiers & Regulatory

Product NDC 60505-4774
Product ID 60505-4774_cc72732d-7d9f-421b-9aff-ffc577aa3e4e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA022567
Marketing Start 2022-06-04
Marketing End 2026-04-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 605054774
Hyphenated Format 60505-4774

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 (source: ndc)
Generic Name vilazodone hydrochloride (source: ndc)
Application Number NDA022567 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (60505-4774-3)
source: ndc

Packages (1)

Ingredients (1)

vilazodone hydrochloride (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cc72732d-7d9f-421b-9aff-ffc577aa3e4e", "openfda": {"unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["fad37b72-1ebe-4a71-835d-b0c1e4b90011"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (60505-4774-3)", "package_ndc": "60505-4774-3", "marketing_end_date": "20260430", "marketing_start_date": "20220604"}], "brand_name": "Vilazodone", "product_id": "60505-4774_cc72732d-7d9f-421b-9aff-ffc577aa3e4e", "dosage_form": "TABLET", "product_ndc": "60505-4774", "generic_name": "vilazodone hydrochloride", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vilazodone", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "NDA022567", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260430", "marketing_start_date": "20220604"}