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Watson Pharmaceuticals, Inc., a leader in generic and specialty branded pharmaceuticals, announced that its subsidiary, Watson Laboratories, Inc., has received final approval from the United States Food and Drug Administration on its Abbreviated New Drug Application (ANDA) for desogestrel/ethinyl estradiol and ethinyl estradiol tablets, 0.15 mg/0.02 mg and 0.01 mg and placebo tablets (28- day regimen). Desogestrel/ethinyl estradiol and ethinyl estradiol tablets, 0.15 mg/0.02 mg and 0.01 mg and placebo tablets (28- day regimen) are the generic equivalent to Duramed Pharmaceuticals' Mircette low-dose monthly oral contraceptive product, which is indicated for prevention of pregnancy.

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