viibryd

Generic: vilazodone hydrochloride

Labeler: allergan, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name viibryd
Generic Name vilazodone hydrochloride
Labeler allergan, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

vilazodone hydrochloride 10 mg/1

Manufacturer
Allergan, Inc.

Identifiers & Regulatory

Product NDC 0456-1110
Product ID 0456-1110_7502bf82-6281-4d90-8471-1450580c4f3c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA022567
Listing Expiration 2026-12-31
Marketing Start 2011-04-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04561110
Hyphenated Format 0456-1110

Supplemental Identifiers

RxCUI
1086772 1086776 1086778 1086780 1086784 1086786 1086789 1086790 1653469 1653470
UPC
0304561120307 0304561140305
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 viibryd (source: ndc)
Generic Name vilazodone hydrochloride (source: ndc)
Application Number NDA022567 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (0456-1110-30)
source: ndc

Packages (1)

Ingredients (1)

vilazodone hydrochloride (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7502bf82-6281-4d90-8471-1450580c4f3c", "openfda": {"upc": ["0304561120307", "0304561140305"], "unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086776", "1086778", "1086780", "1086784", "1086786", "1086789", "1086790", "1653469", "1653470"], "spl_set_id": ["4c55ccfb-c4cf-11df-851a-0800200c9a66"], "manufacturer_name": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (0456-1110-30)", "package_ndc": "0456-1110-30", "marketing_start_date": "20110429"}], "brand_name": "VIIBRYD", "product_id": "0456-1110_7502bf82-6281-4d90-8471-1450580c4f3c", "dosage_form": "TABLET", "product_ndc": "0456-1110", "generic_name": "vilazodone hydrochloride", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VIIBRYD", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA022567", "marketing_category": "NDA", "marketing_start_date": "20110429", "listing_expiration_date": "20261231"}