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Mylan gets US FDA approval for Zaleplon capsules
Pittsburgh | Thursday, June 12, 2008, 08:00 Hrs  [IST]

Mylan Inc, announced that its subsidiary, Genpharm ULC, has received final approval from the US Food and Drug Administration (FDA) for its Abbreviated New Drug Application (ANDA) for Zaleplon capsules, 5 mg and 10 mg.

Zaleplon capsules are the generic version of King Pharmaceuticals' Sonata capsules, which had US sales of approximately $88 million for the 12 months ending March 31, 2008, according to IMS Health.

This product is shipping immediately and will be sold under the Mylan Pharmaceuticals brand.

Mylan Inc., with a presence in more than 90 countries, ranks among the leading diversified generic and specialty pharmaceutical companies in the world.

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