vilazodone hydrochloride

Generic: vilazodone hydrochloride

Labeler: accord healthcare inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name vilazodone hydrochloride
Generic Name vilazodone hydrochloride
Labeler accord healthcare inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

vilazodone hydrochloride 40 mg/1

Manufacturer
Accord Healthcare Inc.

Identifiers & Regulatory

Product NDC 16729-354
Product ID 16729-354_40aa8e57-b9a0-9e45-e063-6294a90ab03e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208209
Listing Expiration 2026-12-31
Marketing Start 2022-06-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16729354
Hyphenated Format 16729-354

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 ANDA208209 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (16729-354-10)
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": "40aa8e57-b9a0-9e45-e063-6294a90ab03e", "openfda": {"unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["f917f30d-f2a7-43eb-836f-53eaa2a31cb0"], "manufacturer_name": ["Accord Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (16729-354-10)", "package_ndc": "16729-354-10", "marketing_start_date": "20220604"}], "brand_name": "Vilazodone Hydrochloride", "product_id": "16729-354_40aa8e57-b9a0-9e45-e063-6294a90ab03e", "dosage_form": "TABLET", "product_ndc": "16729-354", "generic_name": "Vilazodone Hydrochloride", "labeler_name": "Accord Healthcare Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vilazodone Hydrochloride", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA208209", "marketing_category": "ANDA", "marketing_start_date": "20220604", "listing_expiration_date": "20261231"}