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Michael O'Riordan. Mylan received final approval from the FDA on Tuesday, granting the company days of market exclusivity for the production of the 2. Mylan was the first to file for approval of the generic and will receive market exclusivity when the drug is launched or when a final court decision is reached in a patent-litigation dispute with, whichever comes first. In, sued Mylan for patent infringement and that case is currently before a federal court in Pittsburgh, PA. Recently, Teva Pharmaceutical Industries also received tentative approval for 2. Approval is expected upon the expiration of patent https://www.savannahanimalhosprx.com protection for Norvasc in Cite this: Michael O'Riordan. Michael O'Riordan is a journalist for Medscape. Before becoming a journalist for theheart. Michael studied at Queen's University in Kingston and the University of Toronto and has a master's degree in journalism from the University of British Columbia, where he specialized in medical reporting.
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