FdaApplication

NDA 204370

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Identifiers

Properties

PropertyValue
applicant_nameABBVIE INC
application_typeNDA
approval_date2015-09-17

Revenue by product

VRAYLAR

PeriodRevenue
Q2 2026$1.1B
Q1 2026$905.0M
Q4 2025$1.0B
Q3 2025$934.0M
Q2 2025$900.0M
Q1 2025$765.0M
Q4 2024$924.0M
Q3 2024$875.0M
Q2 2024$774.0M
Q1 2024$694.0M
Q4 2023$789.0M
Q3 2023$751.0M
Q2 2023$658.0M
Q1 2023$561.0M
Q4 2022$565.0M
Q3 2022$554.0M
Q2 2022$492.0M
Q1 2022$427.0M
Q4 2021$489.0M
Q3 2021$461.0M
Q2 2021$432.0M
Q1 2021$346.0M
Q4 2020$401.0M
Q3 2020$358.0M
Q2 2020$192.0M
Q1 2020$0.0M
Q4 2019$0.0M
Q3 2019$0.0M
Q2 2019$0.0M

Revenue as this company reported it for this product. A combination product's amount is stated once, for the product, and never divided across its ingredients. A fourth quarter is the reported full year less nine months, since no filing states one.

Products (6)

ProductActive ingredientStrengthDosage form
VRAYLARCARIPRAZINE HYDROCHLORIDEEQ 4.5MG BASECAPSULE;ORAL
VRAYLARCARIPRAZINE HYDROCHLORIDEEQ 6MG BASECAPSULE;ORAL
VRAYLARCARIPRAZINE HYDROCHLORIDEEQ 1.5MG BASECAPSULE;ORAL
VRAYLARCARIPRAZINE HYDROCHLORIDEEQ 0.5MG BASECAPSULE;ORAL
VRAYLARCARIPRAZINE HYDROCHLORIDEEQ 3MG BASECAPSULE;ORAL
VRAYLARCARIPRAZINE HYDROCHLORIDEEQ 0.75MG BASECAPSULE;ORAL

6 products