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Teva Pharmaceutical Industries Ltd. (Nasdaq: TEVA) announced that the U.S. Food and Drug Administration (FDA) has granted final approval for the company's Abbreviated New Drug Application (ANDA) to market its Generic version of GlaxoSmithKline's cardiovascular agent Coreg® (Carvedilol) Tablets, 3.125 mg, 6.25 mg, 12.5 mg and 25 mg. Shipment of this product will begin immediately. [click link for ...

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Teva Provides Update on Generic Famvir(R) Litigation (Finanzen.net)
Teva Pharmaceutical Industries Ltd. (Nasdaq:TEVA) announced today that further to its press release dated September 7, 2007, it has received notice that the United States Court of Appeals for the Federal Circuit has issued an order ...

Teva Provides Update on Generic Famvir(R) Litigation (FinanzNachrichten)
Teva Pharmaceutical ( Nachrichten ) Industries Ltd. (Nasdaq:TEVA) announced today that further to its press release dated September 7, 2007, it has received notice that the United States Court of Appeals for the Federal Circuit has issued an order temporarily enjoining the Company from further sales of generic Famciclovir Tablets, AB-rated to Novartis ' Famvir ® Tablets.

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07/09/2007 16:15:00 Business Wire Teva Pharmaceutical Industries Ltd. (Nasdaq:TEVA) announced today that further to its press release dated September 5, 2007, it has commenced shipment of Famciclovir Tablets, 125 mg, 250 mg and 500 mg, AB-rated to Novartis herpes treatment Famvir(R) Tablets....

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Teva Announces Approval of Generic Famvir(R) Tablets (Business Wire via Yahoo! Finance)
JERUSALEM----Teva Pharmaceutical Industries Ltd. announced today that the U.S. Food and Drug Administration has granted final approval for the Company's Abbreviated New Drug Application to market its generic version of Novartis' Famvir® Tablets, 125 mg, 250 mg and 500 mg.

Doctors in the House: Shingles vaccine may be worth cost (The Cincinnati Post)
Chickenpox was a common viral illness that most of us over age 50 endured when we were kids. One unusual thing about the virus that caused this illness is that after the chickenpox resolved, the virus remained in the nervous system of our bodies in a dormant state.

Are companies calling the shots? (Dayton Daily News)
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Noticias Infobolsa / Titulares (InfoBolsa)
10/08/2007 18:13:00 Business Wire Teva Pharmaceutical Industries Ltd. (Nasdaq: TEVA) announced today that the U.S. Food and Drug Administration has granted tentative approval for the Company s Abbreviated New Drug Application (ANDA) for Sildenafil Citrate Tablets, 20 mg....

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Teva Announces Approval of Generic Protonix(R) Delayed Release Tablets, 20 mg and 40 mg (Business Wire via Yahoo! Finance)
JERUSALEM----Teva Pharmaceutical Industries Ltd. announced today that the U.S. Food and Drug Administration has granted final approval for the Company's Abbreviated New Drug Application to market its generic version of Wyeth's Protonix® Delayed Release Tablets, 20 mg and 40 mg.

Teva Reports Second Quarter 2007 Results (FinanzNachrichten)
Teva Pharmaceutical ( Nachrichten ) Industries Ltd. (Nasdaq: TEVA) today announced its financial results for the second quarter ended June 30, 2007. “This was an excellent quarter for Teva, “ said Shlomo Yanai, Teva ' s President and CEO . “ We are especially pleased with our record-breaking sales figures, which show an increase of 15 percent over last quarter, and 10 percent over the second ......

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