FDA halts marketing of unapproved nitroglycerin tablets - ONA

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FDA halts marketing of unapproved nitroglycerin tablets - ONA

oncologynurseadvisor.com

The FDA has ordered Glenmark Generics and Konec Inc. to stop marketing unapproved nitroglycerin tablets.

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Tags: Angina Medication, FDA, Nitrostat

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Most Recently Shared on March 17, 2010 at 1:47 pm By:

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FDA halts marketing of unapproved nitroglycerin tablets http://goo.gl/fb/qG2x

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FDA Orders 2 Companies To Stop Marketing Unapproved Nitroglycerin Tablets

mnt.to — “The U.S. Food and Drug Administration today ordered Glenmark Generics of Mahwah, N.J., and Konec Inc. of Tucson, Ariz., to stop marketing unapproved nitroglycerin tablets. The tablets are placed uView full resource at mnt.to

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Most Recently Shared on March 18, 2010 at 1:31 am By:

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MedicalNewsToday: FDA Orders 2 Companies To Stop Marketing Unapproved Nitroglycerin Tablets http://bit.ly/9EklAK Full http://bit.ly/bhL2V3

2 years ago...

FDA Orders 2 Companies To Stop Marketing Unapproved Nitroglycerin Tablets

medicalnewstoday.com — “The U.S. Food and Drug Administration today ordered Glenmark Generics of Mahwah, N.J., and Konec Inc. of Tucson, Ariz., to stop marketing unapproved nitroglycerin tablets. The tablets are placed uView full resource at medicalnewstoday.com

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Most Recently Shared on March 18, 2010 at 1:07 am By:

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FDA Orders 2 Companies To Stop Marketing Unapproved Nitroglycerin Tablets The U.S. Food and Drug Administration today.. http://bit.ly/9ESV3B

2 years ago...

FDA Orders 2 Companies to Stop Marketing Unapproved Nitroglycerin Tablets

fda.gov — “The U.S. Food and Drug Administration today ordered Glenmark Generics of Mahwah, N.J., and Konec Inc. of Tucson, Ariz., to stop marketing unapproved nitroglycerin tablets. The tablets are placed under the tongue to relieve chest pain or to stop a heart attack and are marketed in 0.3 mg, 0.4 mg, and 0.6 mg dosages.View full resource at fda.gov

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FDA Orders 2 Companies to Stop Marketing Unapproved Nitroglycerin Tablets. http://bit.ly/9uJmS2

2 years ago...

FDA Acts To Halt Marketing Of Unapproved Codeine Sulfate Tablets

medicalnewstoday.com — “The U.S. Food and Drug Administration warned four companies that they must stop marketing unapproved codeine sulfate tablets. These drugs are opioid analgesics, commonly called narcotics, that areView full resource at medicalnewstoday.com

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Most Recently Shared on October 14, 2009 at 1:40 pm By:

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FDA Acts To Halt Marketing Of Unapproved Codeine Sulfate Tablets: The U.S. Food and Drug Administration warned .. http://bit.ly/3rdVcM

3 years ago...

FDA Acts to Halt Marketing of Unapproved Codeine Sulfate Tablets

fda.gov — “The U.S. Food and Drug Administration today warned four companies that they must stop marketing unapproved codeine sulfate tablets. These drugs are opioid analgesics, commonly called narcotics, that are widely used to treat pain.View full resource at fda.gov

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FDA Acts to Halt Marketing of Unapproved Codeine Sulfate Tablets http://bit.ly/9SeQ6

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