<?xml version="1.0" encoding="UTF-8" ?>
<Journal>
<Journal-Info>
<name>PHARMANEST : An International Journal of Advances in Pharmaceutical Sciences</name>
<website>pharmanest.net</website>
<email>pharmanest@gmail.com</email>
<issn mediatype='print'> 2453-7005 Online: 2343-212X</issn>
<issn mediatype='Online'></issn>
</Journal-Info>
<article>
<title>FORMULATION AND EVALUATION OF EFAVIRENZ TABLETS DEVELOPED BY MOISTURE ACTIVATED DRY GRANULATION</title>
<authors>P.NITHIN*</authors>
<keywords>Efavirenz, NNRTI, Formulation, Evaluation, MADG.</keywords>
<pages>1361-1382</pages>
<issue_number>Volume 4, Issue 6</issue_number>
<issue_period>November - December 2013</issue_period>
<abstract>The aim of present work is to formulate and evaluate efavirenz tablets. Efavirenz tablets were prepared by using Moisture Activated Dry Granulation. Efavirenz is a nonnucleoside reverse transcriptase inhibitor (NNRTI) used to treat HIV-1 infection and AIDS. As with other anti-retroviral drugs, HIV rapidly develops resistance if efavirenz is used alone. So recommended therapy consists of combinations of three or more anti-retroviral. Objective is to monitor the manufacturing process of efavirenz tablets to facilitate the formulation, evaluation, optimization and confirmation of the critical product / process parameter identified during the developmental stage of the formulation so that the final product at pilot scale / test batch will produce consistent results.</abstract>
</article>
</Journal>
