Logos are each company's own site icon, matched by name through Wikidata.Company names and logos identify the companies in public FDA and registry records and do not imply endorsement.
Sold as Intelence. Every FDA application for this active ingredient: 1 branded and 3 generic.
As of Nov 15, 2026, FDA lists 4 applications for Etravirine (sold as Intelence), first approved Jan 18, 2008, with 4 new uses approved and 0 published complete response letters.
First approved: Jan 18, 2008
Applications: 4
New uses approved: 4
Complete response letters: 0
Medicare spending, 2025: $20.2M
First approved in the EU: Aug 28, 2008
First approved in Japan: Dec 25, 2008
Medicare Spending
CMS Part D and Part B, 2025, before manufacturer rebates; matched by generic name
Etravirine
Part D
$18.6M
-18%
2,125
Intelence
Part D
$1.7M
-32%
191
What Pharmacies Pay
Median price per unit across package codes in CMS's weekly NADAC survey, Nov 11, 2026, before rebates; see every drug's price change
ETRAVIRINE 100 MG TABLET: $7.77 per unitGeneric · -2% in a year
ETRAVIRINE 200 MG TABLET: $9.24 per unitGeneric · -19% in a year
INTELENCE 200 MG TABLET: $24.30 per unitBrand · +0% in a year
Approvals in the EU (EMA)
First approved in the EU 7 months after the US. Centrally authorised medicines, matched by ingredient; see all EU approvals
First approved in Japan 11 months after the US. PMDA's English list since 2008, matched by ingredient; see all Japanese approvals
Intelence, new ingredientA drug containing a new active ingredient indicated for the treatment of HIV-1 infection. · Janssen Pharmaceutical K.K. · Dec 25, 2008
Applications, approvals and products come from FDA's Drugs@FDA data files, refreshed weekly, grouped by active ingredient as FDA spells it. Complete response letters are FDA's published letters. Medicare spending is CMS's Part D and Part B dashboard, matched to this ingredient by generic name; shortages are FDA's shortage list, matched by application number; clinical trials are ClinicalTrials.gov studies naming the ingredient as an intervention, refreshed daily; safety programs are FDA's REMS list, matched by application number or, for shared programs, by ingredient.Drugs@FDA
