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United States · US · US:0456-1120_7502bf82-6281-4d90-8471-1450580c4f3c
VIIBRYD
Orange BookUNIISPLATC N06AX24
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAllergan, Inc.
CountryUS (United States)
ATC codeN06AX24
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11045611203030 TABLET in 1 BOTTLE (0456-1120-30)
Annotations
UNII (FDA Substance ID)
U8HTX2GK8J
VILAZODONE HYDROCHLORIDE
RxCUI 1086768
Orange Book
N022567
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "U8HTX2GK8J",
"rxcui": "1086768",
"inchikey": "RPZBRGFNBNQSOP-UHFFFAOYSA-N",
"display_name": "VILAZODONE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"4c55ccfb-c4cf-11df-851a-0800200c9a66": {
"match": "brand_token",
"title": "VIIBRYD (VILAZODONE HYDROCHLORIDE) TABLET VIIBRYD (VILAZODONE HYDROCHLORIDE) KIT [ALLERGAN, INC.]",
"spl_version": "34",
"published_date": "2025-12-22"
}
},
"productid": "0456-1120_7502bf82-6281-4d90-8471-1450580c4f3c",
"productndc": "0456-1120",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "022567",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "10MG",
"product_no": "001",
"approval_date": "Jan 21, 2011"
},
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "20MG",
"product_no": "002",
"approval_date": "Jan 21, 2011"
},
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "40MG",
"product_no": "003",
"approval_date": "Jan 21, 2011"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "VILAZODONE HYDROCHLORIDE",
"proprietary_name": "VIIBRYD",
"active_ingred_unit": "mg/1",
"application_number": "NDA022567",
"marketing_category": "NDA",
"nonproprietary_name": "vilazodone hydrochloride",
"start_marketing_date": "20110429",
"active_numerator_strength": "20"
}Related drugs
Other records sharing ATC code N06AX24.
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