Friday, May 30, 2008

The U.S. Food and Drug Administration

Lilly Submits Cymbalta(R) Supplemental New Drug Application for ...
CNNMoney.com - USA
Eli Lilly and Company (NYSE: LLY) has submitted a supplemental New Drug Application (sNDA) to the US Food and Drug Administration (FDA) seeking approval for ...
See all stories on this topic

US FDA approves Glenmark's metformin tablets
Reuters India - Mumbai,India
MUMBAI (Reuters) - The US Food and Drug Administration has approved Glenmark Pharmaceuticals Ltd's diabetes drug metformin hydrochloride tablets in multiple ...
See all stories on this topic

Dr Reddy's gets tentative US FDA nod for omeprazole
Reuters - USA
N: Quote, Profile, Research) has received tentative approval from the US Food and Drug Administration for omeprazole delayed-release capsules, ...
See all stories on this topic

50000 Irish use anti-smoking drug linked to suicides in US
Irish Independent - Dublin,Ireland
... in the US in an attempt to allay concerns over the drug, sales of which have slumped by one-third since the US Food and Drug Administration watchdog ...
See all stories on this topic

UPDATE 1-Glaxo seeks US approval for anti-nausea drug
Reuters India - Mumbai,India
The stock was hit by worries about prospects for another new drug, Promacta, following negative comments from a US Food and Drug Administration reviewer. ...
See all stories on this topic

UPDATE 1-US delays OK to broaden use of Wyeth antibiotic
Reuters - USA
In issuing its "approvable letter," the US Food and Drug Administration also requested information about potential liver toxicity with Tygacil. ...
See all stories on this topic

US Attorney - Wholesale Pharmaceutical Company Owner Sentenced On ...
Lawfuel (press release) - Wellington,New Zealand
Mr. Acosta commended the investigative efforts of the US Food and Drug Administration. This case was prosecuted by Assistant United States Attorneys Lois ...
See all stories on this topic

Blogs Alert for: The U.S. Food and Drug Administration

Lilly Submits Cymbalta® Supplemental New Drug Application For ...
Eli Lilly and Company has submitted a supplemental New Drug Application (sNDA) to the US Food and Drug Administration (FDA) seeking approval for a new indication for Cymbalta (duloxetine HCl) for the management of chronic pain, ...
Pharmaceutical Online Home Page - http://www.pharmaceuticalonline.com/

The Sentinel Initiative: A National Strategy for Monitoring ...
By Shirl Kennedy
The US Food and Drug Administration of the 21st century needs such an electronic system to serve as sentinel over the safety of medical products and help FDA fulfill its responsibility to protect the health and well being of the ...
Docuticker - http://www.docuticker.com

The World According to Monsanto - Great Video on Monsanto GM Crops
By Vox Populae
One example is Michael Taylor, who worked for Monsanto as an attorney before being appointed as deputy commissioner of the US Food and Drug Administration (FDA) in 1991. While at the FDA, the authority that deals with all US food ...
Vanguard News Network Forum - http://www.vnnforum.com

Lilly Submits Cymbalta(R) Supplemental New Drug Application for ...
Lilly Submits Cymbalta(R) Supplemental New Drug Application for Chronic Pain to US Food and Drug Administration.
FOXBusiness.com - http://www.foxbusiness.com

No comments: