Wednesday, July 8, 2026

Drug profile · INN

emtricitabine, tenofovir alafenamide

emtricitabine, tenofovir alafenamide (EMTRICITABINE AND TENOFOVIR ALAFENAMIDE) is an FDA-listed pharmaceutical active ingredient. Route of administration: oral. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 1
News articles 0
Drug details — emtricitabine, tenofovir alafenamide
US status
approved
Class
Route
ORAL
Patents
0
Programs
1
Data quality
0.84

Quick answer

emtricitabine, tenofovir alafenamide (EMTRICITABINE AND TENOFOVIR ALAFENAMIDE) is an FDA-listed pharmaceutical active ingredient. Route of administration: oral. Current US regulatory status: approved.

Key facts

INN emtricitabine, tenofovir alafenamide
Brand EMTRICITABINE AND TENOFOVIR ALAFENAMIDE
Route ORAL
Formulation TABLET

Approval history

Authority Status Date
FDA approved

Pipeline programs

  1. emtricitabine/tenofovir alafenamide Phase 2 · United Therapeutics Europe · Acceptability of Health Care

Frequently asked questions

What is emtricitabine, tenofovir alafenamide?

emtricitabine, tenofovir alafenamide (EMTRICITABINE AND TENOFOVIR ALAFENAMIDE) is an FDA-listed pharmaceutical active ingredient. Route of administration: oral. Current US regulatory status: approved.

What is the brand name for emtricitabine, tenofovir alafenamide?

EMTRICITABINE AND TENOFOVIR ALAFENAMIDE is a marketed brand name for emtricitabine, tenofovir alafenamide. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of emtricitabine, tenofovir alafenamide?

emtricitabine, tenofovir alafenamide has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.