<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>Pharmaceutical Product Guide &#187; antipsychotic</title>
	<atom:link href="http://www.pharmaceuticalproductguide.com/blog/tag/antipsychotic/feed/" rel="self" type="application/rss+xml" />
	<link>http://www.pharmaceuticalproductguide.com/blog</link>
	<description>A comprehensive guide to pharmaceutical products for medical professionals</description>
	<lastBuildDate>Fri, 11 Jun 2010 09:15:33 +0000</lastBuildDate>
	<generator>http://wordpress.org/?v=2.8.2</generator>
	<language>en</language>
	<sy:updatePeriod>hourly</sy:updatePeriod>
	<sy:updateFrequency>1</sy:updateFrequency>
			<item>
		<title>Teva sues FDA after denial of generic Risperdal exclusivity</title>
		<link>http://www.pharmaceuticalproductguide.com/blog/2008/03/25/teva-sues-fda-after-denial-of-generic-risperdal-exclusivity/</link>
		<comments>http://www.pharmaceuticalproductguide.com/blog/2008/03/25/teva-sues-fda-after-denial-of-generic-risperdal-exclusivity/#comments</comments>
		<pubDate>Tue, 25 Mar 2008 15:17:06 +0000</pubDate>
		<dc:creator>Kimberly O'Brien</dc:creator>
				<category><![CDATA[Lawsuits]]></category>
		<category><![CDATA[antipsychotic]]></category>
		<category><![CDATA[generic Risperdal]]></category>
		<category><![CDATA[Teva]]></category>

		<guid isPermaLink="false">http://www.pharmaceuticalproductguide.com/blog/2008/03/25/teva-sues-fda-after-denial-of-generic-risperdal-exclusivity/</guid>
		<description><![CDATA[Teva Pharmaceuticals has filed a lawsuit in a U.S. district court against the FDA after being denied the 180-day exclusivity for its generic version of the blockbuster antipsychotic Risperdal. Teva said that it was eligible for the 180-day marketing exclusivity, as it was the first to submit an abbreviated new drug application (ANDA) for Janssen [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://www.tevapharm.com/">Teva Pharmaceuticals</a> has filed a lawsuit in a U.S. district court against the FDA after being denied the 180-day exclusivity for its generic version of the blockbuster antipsychotic Risperdal. Teva said that it was eligible for the 180-day marketing exclusivity, as it was the first to submit an abbreviated new drug application (ANDA) for Janssen Pharmaceutical’s Risperdal (risperidone) tablets with a Paragraph IV certification for the ’952 patent.</p>
]]></content:encoded>
			<wfw:commentRss>http://www.pharmaceuticalproductguide.com/blog/2008/03/25/teva-sues-fda-after-denial-of-generic-risperdal-exclusivity/feed/</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
	</channel>
</rss>
