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For Consumers

Tentative approval of Efavirenz/Emtricitabine/Tenofovir Disoproxil Fumarate

On August 12, 2009, FDA granted tentative approval for a generic fixed dose combination product containing efavirenz/emtricitabine/fenofovir disoproxil fumarate 600 mg/200 mg/300 mg manufactured by Matrix Laboratories Limited of Hyberdad, India. It is indicated for use alone or in combination with other antiretroviral products for the treatment of HIV-1 infection in adults.

"Tentative approval" means that FDA has concluded that a drug product meets all required quality, safety and efficacy standards, but is not presently eligible for final approval or marketing in the U.S. because of existing patents and/or exclusivity rights. However, tentative approval does make the product eligible for purchase outside the United States under the President’s Emergency Plan for AIDS Relief (PEPFAR).

As with all generic applications, FDA conducts an on-site inspection of each manufacturing facility, and of the facilities performing the bioequivalence studies, to evaluate the ability of the manufacturer to produce a quality product and to assess the quality of the bioequivalence data supporting the application prior to granting approval or tentative approval to these applications.

The product is a generic formulation of Atripla Tablets, 600 mg/200 mg/300 mg of Gilead Sciences Inc., which is subject to various patent protections.

Patent information is available for this and other approved products in FDA's Approved Drug Products with Therapeutic Equivalence Evaluations(the “Orange Book”)

A complete list of all  Approved and Tentatively Approved Antiretrovirals in Association with the President's Emergency Plan is available on the FDA web site.

Richard Klein
Office of Special Health Issues
Food and Drug Administration

Kimberly Struble
Division of Antiviral Drug Products
Food and Drug Administration

Page Last Updated: 08/20/2014
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