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LUPIN LTD. - Lupin Ltd reply to clarification sought by the exchange
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26 May 2015
The Exchange had sought clarification from Lupin Ltd with respect to news article appearing in Financial Express on May 22, 2015 titled &quot;Some drugs made by Lupin, DRL &amp; Mylan lose EU approval&quot;&lt;BR&gt;&lt;BR&gt;Lupin Ltd replied stating &quot;We wish to state that in connection with GVK Bio Eqivalence(&apos;BE&apos;) studies, the Company along with many other companies in the EU received communication from European Medicines Agency (&apos;EMA&apos;) for suspension of Trimetazidine MR 35mg. tablets and Cefpodoxime 200mg. tablets in January 2015.&lt;BR&gt; &lt;BR&gt;The Company informed the EMA that it will submit new BE studies for Trimetazidine MR 35mg. tablets and Cefpodoxime 200mg. tablets to EMA by June 2015.&lt;BR&gt; &lt;BR&gt;The Company has successfully conducted the new BE studies for the said Products and submitted the report in May 2015 for review by EMA.&quot;
View all announcements for LUPIN LTD. Source: BSE India