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Glenmark Pharmaceuticals gets ANDA approval for Norethindrone Acetate and Ethinyl Estradiol Tablets

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Capital Market

From USFDA

Glenmark Pharmaceuticals announced that it has been granted final approval by United States Food & Drug Administration for Norethindrone Acetate and Ethinyl Estradiol Tablets USP, 1 mg/0.02 mg, the generic version of Loestrin 21 1/20 Tablets of Warner Chilcott Company, LLC.

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First Published: Jan 21 2016 | 10:15 AM IST

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