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Impax Labs gets final US FDA nod for generic Depakote ER 500mg tabs
Hayward, California | Friday, August 7, 2009, 08:00 Hrs  [IST]

Impax Laboratories, Inc. confirmed that the US Food and Drug Administration (FDA) has granted final approval of the company's Abbreviated New Drug Application (ANDA) for generic version of Depakote (divalproex ER) 500mg extended-release tablets. The company received approval on the 250mg tablets in May 2009. Abbott Laboratories markets Depakote ER for the treatment of epilepsy and bipolar disorders.

The company expects to launch both the 250mg and 500mg tablets immediately, through Global Pharmaceuticals, Impax's generic division.

According to Wolters Kluwer Health, US sales of Depakote ER 250mg and 500mg tablets were approximately $93 million and $633 million, respectively, for the 12 months ended June 30, 2009.

Impax Laboratories, Inc. is a technology based specialty pharmaceutical company applying its formulation expertise and drug delivery technology to the development of controlled-release and specialty generics in addition to the development of branded products.

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