Watson challenges Takeda's Rozerem patent
AP - 40 minutes agoWatson Pharmaceuticals Inc. said Friday it is challenging Takeda Pharmaceutical Co.'s patent on the insomnia treatment Rozerem.
Food and Drug Administration
4783 Stories, most recent news story added 37 minutes ago
News Stories
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Targacept, AstraZeneca cooperate on depression med
AP via Yahoo! News - Thu Dec 3, 10:38 am ETTargacept Inc. on Thursday struck a deal potentially worth more than $1 billion to develop a depression drugs with AstraZeneca PLC, one of the world's largest drugmakers.
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Man wanted in death of toddler is arrested
The Charlotte Observer - Fri Dec 4, 6:34 am ETA 19-year-old man wanted in connection with the death of a 22-month-old girl he was baby-sitting last weekend was arrested Wednesday night, Charlotte-Mecklenburg police said.
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ICON Receives Warning Letter Relating to Two Studies
Business Wire via Yahoo! Finance - 1 hour 6 minutes agoDUBLIN----ICON plc, , today announced it has received a warning letter from the U.S. Food and Drug Administration regarding clinical study management services provided by the company to one of its clients in relation to two studies conducted between 2004 and 2006.
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Endo says FDA asked for info on Aveed side effects
San Francisco Chronicle - Thu Dec 3, 2:39 pm ETEndo Pharmaceuticals Holdings Inc. said Thursday regulators want more information about its testosterone injection Aveed as they consider approving the drug for sale. Endo said the FDA sent a complete response letter asking for details about rare but serious... Food and Drug Administration - Drug - Adverse effect - Health - Business
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FDA announces Chinese herb recall
UPI - Thu Dec 3, 9:48 am ETWASHINGTON, Dec. 3 (UPI) -- The U.S. Food and Drug Administration announced the recall of Radix Polygonati Officinalis, a Chinese herb, because of a labeling error.
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St. Jude Medical Receives FDA Approval for Industry-First Five-Column Neurostimulation Lead to Manage Chronic Pain
Business Wire via Yahoo! Finance - 2 hours 6 minutes agoST. PAUL, Minn.----St. Jude Medical, Inc. today announced the U.S. Food and Drug Administration approval and U.S. market introduction of its new Penta™ surgical lead for neurostimulation therapy.
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Kin sue Harvard over son’s suicide
Boston Globe - Fri Dec 4, 12:58 am ETHarvard sophomore John Edwards was studying to become a doctor and training for the Boston Marathon in June 2007 when he sought help at the university’s Health Services because he could not study for as many hours as some of his friends.
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Seed success slows approval process
The Des Moines Register - Fri Dec 4, 5:21 am ETExecutives of the three leading corn and soybean seed companies said Thursday that the pace of federal regulatory approvals for biotech seeds, once granted at almost breakneck speed, has slowed in recent years.
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London afternoon: Stocks bounce into the blue after US jobs
ShareCast - 37 minutes agoLONDON (SHARECAST) - Share prices have surged higher as the keenly watched US monthly jobs figures showed a big drop in the number losing their jobs and an unexpected drop in the level of US unemployment.
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Sector movers: US jobs data boosts miners
ShareCast - 52 minutes agoLONDON (SHARECAST) - Mining stocks have stormed ahead after some surprisingly upbeat jobs data from the US.
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Recalled cat food came from plant in Gaston
The Post and Courier - 59 minutes agoCOLUMBIA -- An executive of Diamond Pet Foods, which announced a recall of two varieties of cat food, said Thursday that the tainted products were manufactured at the same Gaston plant that in 2005 produced a toxic dog food responsible for the deaths or illnesses of dozens of dogs around the nation.
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US FDA Approves SEROQUEL XR(R) For Add-On Treatment of Major Depressive Disorder
PR Newswire via Yahoo! Finance - Fri Dec 4, 7:00 am ETAstraZeneca today announced that the US Food and Drug Administration has approved once-daily SEROQUEL XR® Extended Release Tablets as adjunctive treatment to antidepressants in adults with Major Depressive Disorder .
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FDA approves hereditary angioedema drug
UPI - Thu Dec 3, 7:59 am ETWASHINGTON, Dec. 3 (UPI) -- The U.S. Food and Drug Administration says it has approved a drug called Kalbitor to treat people suffering from hereditary angioedema.
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TSO3 receives FDA's clearance for expanded use
CNW Group via Yahoo! Finance - Fri Dec 4, 6:00 am ETTSO3 Inc. , an innovator in low temperature sterilization technology for medical devices in healthcare settings through the use of ozone, today announced that the Company has received clearance from the US Food and Drug Administration to expand the intended use claims for its TSO3 STERIZONE 125L Sterilizer.
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Nassco completes oil tanker 11 months ahead of schedule
San Diego Union-Tribune - Fri Dec 4, 3:19 am ETNassco, a General Dynamics shipyard in San Diego, delivered the third oil tanker manufactured for American Petroleum Tankers LLC, a joint venture of the Blackstone Group.
FDA: Recalls
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Snax in Pax, Inc. Issues a Nationwide Allergy Alert on Undeclared Milk Allergen in Caramel Corn and Caramel Puff Products.
Fri Dec 4, 8:50 am EST -
Sunny Lake Trading Inc. Issues Alert on Undeclared Sulfites in Radix Polygonati Officialis
Thu Dec 3, 8:51 am EST -
Rikki USA, Inc.Re-Issues Allergy Alert on Undeclared Shrimp in Toi Sauce Thai Red Curry (Panang) produced for the Siamrica Co. to Correct Lot Number
Tue Dec 1, 3:52 pm EST -
Diamond Pet Foods Announces Recall of Premium Edge Adult Cat and Premium Edge Hairball Cat Food
Tue Dec 1, 10:11 am EST -
La Espiga De Oro, Inc. Issues Allergy Alert on Undeclared Whey in Flour Tortillas
Tue Dec 1, 8:57 am EST
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