Brimonidine tartrate ophthalmic solution 0.1% and 0.15% (ALPHAGAN): Innovator announced favorable decision by US court
Innovator Allergan announced (in a press release Here ) that the United States District Court for the District of Delaware has ruled in favor of Allergan on key patents covering Brimonidine tartrate ophthalmic solution 0.1% and 0.15% (ALPHAGAN). The court has upheld the validity of key patents US6627210; US6641834; US6673337; US6562873; and US5424078
Fenofibrate (Tricor) 48 mg and 145 mg Tablets: Impax Laboratories Confirms Patent Challenge
Generic player Impax Laboratories confirmed ( in a press release Here) that it has initiated a challenge of the patents listed by Abbott Laboratories in connection with Fenofibrate (Tricor) 48 mg and 145 mg Tablets.
Glatiramer acetate injection (Copaxone):Teva asserts 3 more patents against generic players Monenta/Sandoz
Innovator Teva Pharma announced (in a press release Here) it is seeking to amend its existing complaint against Momenta Pharmaceuticals, Inc./Sandoz Inc. to include patent infringement of three additional patents related to the characterization of Glatiramer acetate injection (Copaxone). The proposed updated complaint has been filed under seal with the U.S. District Court for the Southern District of New York along with a motion requesting that the Court grant Teva leave to amend.
Lansoprazole (Prevacid) Delayed-Release Capsules 15 mg and 30 mg: Teva got final approval
Generic player Teva Pharma announced (in a press release Here) today that the U.S. Food and Drug Administration has granted final approval for the Company's Abbreviated New Drug Application (ANDA) to market its generic version of Tap Pharmaceutical's proton pump inhibitor Lansoprazole (Prevacid) Delayed-Release Capsules 15 mg and 30 mg. Customers will begin receiving product on November 11, 2009. Annual sales of Prevacid® Delayed-Release Capsules were approximately $2.97 billion in the United States for the twelve months that ended June 30, 2009 based on IMS sales data
Generic player Teva Pharma announced (in a press release Here) today that the U.S. Food and Drug Administration has granted final approval for the Company's Abbreviated New Drug Application (ANDA) to market its generic version of Tap Pharmaceutical's proton pump inhibitor Lansoprazole (Prevacid) Delayed-Release Capsules 15 mg and 30 mg. Customers will begin receiving product on November 11, 2009. Annual sales of Prevacid® Delayed-Release Capsules were approximately $2.97 billion in the United States for the twelve months that ended June 30, 2009 based on IMS sales data
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