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Watson Files ANDA For Generic LoSeasonique

Watson Pharmaceuticals has confirmed that its subsidiary, Watson Laboratories, has filed an Abbreviated New Drug Application (ANDA) with the FDA seeking approval to market its levonorgestrel and ethinyl

Genentech Gets FDA Approval For Actemra

The company claims that Actemra is the first interleukin-6 (IL-6) receptor-inhibiting monoclonal antibody approved to treat RA, and may be used alone or in combination with methotrexate or