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FDA approves Watson ANDA for Kadian

Watson Pharmaceuticals has received US FDA approval for its Abbreviated New Drug Application (ANDA) for morphine sulfate extended-release capsules USP, the generic equivalent of Actavis' Kadian.

Kadian is used for management of moderate to severe pain that lasts for an extended period of time.

Following the approval, the company has started shipping the product.

According to a data by IMS Health, Kadian had registered sales of around $275m in the last twelve months ending 30 September 2011.