For second time, FDA delays an approval decision on Questcor's drug Acthar for the treatment of infantile spasms.

LAKE FOREST, Calif.--(BUSINESS WIRE)--ReVision Optics (RVO), a leading company in the research, development and manufacture of implantable medical devices designed to assist patients that need reading glasses, announced today that it has completed enrollm

from green tea and vitamin C" on its can, because the ingredients in the soda "are not nutrients with recognized antioxidant activity." Unilever and the Dr. Pepper Snapple Group, the makers of the two beverages,

drugstorenews.com (US) FDA to discuss concerns over medicines with DXM FDA approves Reckitt Benckiser's Suboxone (Wed Sep 08 12:34:43 2010 PDT)

(AP:ALLEGAN, Mich.) Perrigo Co. said Wednesday it received Food and Drug Administration approval to make a generic version of Aldara Cream, which is used to treat precancerous skin spots.

FRANKLIN, Tenn.--(BUSINESS WIRE)--BMTI completed its 100 day PMA meeting with the FDA regarding the review of Augment'„¢. No unexpected issues were raised that would impact timing. Augment Injectable will be reviewed as medical device.

WESTBOROUGH, Mass. -- Viking Systems, Inc. announced today that it has received clearance of its 510 application by the Food and Drug Administration related to its Next Generation 3DHD visualization system.

MORRISTOWN, N.J. - Watson Pharmaceuticals Inc. said Tuesday it received marketing approval for a generic version of Bayer's oral contraceptive Yasmin. Watson said it has started shipping the drug under the brand

Bayer To Continue Case Vs Watson After FDA OKs Generic Yasmin

dexamethasone in patients with relapsed multiple myeloma. The company has an agreement with the U.S. FDA on a Special Protocol Assessment (SPA) and received Scientific Advice from the European Medicines Agency

Forest Laboratories, Inc. (NYSE: FRX) announced that the U.S. Food and Drug Administration's (FDA) Anti-Infective Drugs Advisory Committee voted 21 - 0 in favor of approval of ceftaroline fosamil for the treatment of

is as safe to eat as food from other Atlantic salmon," the FDA staff wrote in a briefing document. Those findings will be presented Sept. 19 to a panel of scientific experts that will advise top officials at the

(RTTNews) - Forest Laboratories, Inc. (FRX: News ), Tuesday said the U.S. Food and Drug Administration's Anti-Infective Drugs Advisory Committee voted 21 - 0 in favor of approval of ceftaroline fosamil for the