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Some of the Overseas Pharmacy prices: |
Some of the Worldwide Pharmacy prices: |
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BEST SELLERS |
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INSOMNIA Ambien (brand name) and zolpidem (generic Ambien) |
TOO MUCH ACID IN STOMACH (ulcers, reflux disease - GERD or heartburn) Nexium (brand name) and esomeprazole (generic Nexium)Prevacid (brand name) and lansoprazole (generic Prevacid)Prilosec (brand name) and omeprazole (generic Prilosec)Protonix (brand name) and pantoprazole (generic Protonix)Zantac (brand name) and ranitidine (generic Zantac) |
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MIGRAINES AND HEADACHES Imitrex (brand name) and sumatriptan (generic Imitrex) |
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FERTILITY Clomid (brand name) and clomiphene (generic Clomid) |
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NARCOLEPSY Modalert (brand name) and modafinil (generic Modalert) |
ERECTILE DYSFUNCTION (ED)- IMPOTENCE Viagra (brand name) and sildenafil citrate (generic Viagra) |
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• Thu, Jul 2, 2009 -
FDA Approves Multaq to Treat Heart Rhythm Disorder. The U.S. Food and Drug Administration has approved Multaq tablets (dronedarone) to help maintain normal heart rhythms in patients with a history of atrial fibrillation or atrial flutter (heart rhythm disorders). The drug is approved to be used in patients whose hearts have returned to normal rhythm or who will undergo drug or electric-shock treatment to restore a normal heart beat. • Wed, Jul 1, 2009 - FDA: Boxed Warning on Serious Mental Health Events to be Required for Chantix and Zyban. The U.S. Food and Drug Administration today announced that it is requiring manufacturers to put a Boxed Warning on the prescribing information for the smoking cessation drugs Chantix (varenicline) and Zyban (bupropion). The warning will highlight the risk of serious mental health events including changes in behavior, depressed mood, hostility, and suicidal thoughts when taking these drugs. • Tue, Jun 30, 2009 - FDA Seeks Public Input on Tobacco Regulation. The U.S. Food and Drug Administration announced today that it is seeking public input on the implementation of its historic new authority overseeing tobacco products in the United States. In a Federal Register notice, the agency invites the public to provide information and share views on a wide range of topics, from product content to advertising and marketing. • Tue, Jun 30, 2009 - FDA Confirms E. Coli O157:H7 in Prepackaged Nestlé Toll House Refrigerated Cookie Dough. Today, the U.S. Food and Drug Administration announced that it has found E. coli O157:H7 (a bacterium that can cause serious food borne illness) in a sample of prepackaged Nestlé Toll House refrigerated cookie dough currently under recall by the manufacturer and marketer, Nestlé USA. The contaminated sample was collected at Nestlé?s facility in Danville, Va. on June 25, 2009. |
• What are Generic Drugs? - FDA information about generic drugs
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FDA Q&A about generic drugs |