Teva reaches compromise on epinephrine injector

Under the settlement with Pfizer and Mylan, Teva will be allowed to market its generic injector by mid-2015.

Pfizer Inc. (NYSE: PFE) and Mylan Inc. (NYSE: MYL) have announced that Mylan subsidiary Meridian Medical Technologies Inc. has settled patent-infringement litigation with Teva Pharmaceutical Industries Ltd. (Nasdaq: TEVA; TASE: TEVA) over Teva's generic version of the EpiPen device for injecting epinephrine during potentially fatal allergic reactions.

Under the settlement, Teva may begin marketing its version of the injector on June 22, 2015, or earlier under certain circumstances, provided that Teva obtains US Food and Drug Administration (FDA) approval.

Teva does not yet have FDA approval for its generic EpiPen injector, but the settlement settles the legal dispute over its Abbreviated New Drug Application (ANDA) filing with the FDA. Meridian manufactures the EpiPen for Pfizer, and Mylan markets it in the US.

Mylan and Pfizer added that additional details of settlement are confidential, and subject to review by the US Justice Department and the Federal Trade Commission.

In a separate statement, Antares Pharma Inc. (NYSE: AIS), a manufacturer of small-needle injector systems, announced that it will supply Teva with injectors, if needed, for 2013 and 2014, following FDA approval of Teva's ANDA.

Teva's share price was flat at NIS 171.20 in early trading on the TASE today, after remaining unchanged at $45.63 on Nasdaq on Friday, giving a market cap of $43 billion.

Published by Globes [online], Israel business news - www.globes-online.com - on April 29, 2012

© Copyright of Globes Publisher Itonut (1983) Ltd. 2012

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