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Recent related articles ( fda):

FDA Approves Tapentadol As Pain Reliever
Johnson & Johnson Pharmaceutical Research and Development LLC announced today that FDA approved the marketing of tapentadol immediate-release tablets for the relief of moderate to severe acute pain in adults.
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Mylan receives FDA approval for Fluoxetine capsules
Mylan Inc. has announced that its subsidiary, Mylan Pharmaceuticals Inc., received final approval from the U.S. Food and Drug Administration (FDA) for its Abbreviated New Drug Application (ANDA) for Fluoxetine Capsules USP, 10 mg and 20 mg.
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Kaiser Daily Health Policy Report Highlights News Coverage Of Prospects For FDA, Rule Changes On Health Care Issues In New Administration
Summaries of several recent developments related to prospects for FDA and rule changes on health care issues in the new administration of President-elect Barack Obama appear below.FDA: Obama could seek to increase FDA oversight of imported foods and medications and expand the authority of the
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Possibilities For HHS Secretary, FDA Commissioner In Obama Administration Discussed
Democratic congressional staffers and others have begun “floating names for top health posts” in the administration of President-elect Barack Obama that include several possibilities for HHS secretary, the Wall Street Journal’s ” More: continued here
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CNSystems Medizintechnik AG Receives FDA Approval For CNAP? Blood Pressure Monitor 500
CNSystems Medizintechnik AG, a medical device company marketing CNAP?, today announced that the U.S. Food and Drug Administration has cleared the 510(k) notification for CNSystem’s CNAP? Monitor 500, permitting the sale of this product in the United States. The CNAP? Monitor 500 measures non-invasive and continuous
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FDA approves Ranexa for the treatment of chronic angina
CV Therapeutics, Inc. has announced that the U.S. Food and Drug Administration (FDA) has approved a new, first line indication for Ranexa(R) (ranolazine extended-release tablets) for the treatment of chronic angina.
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