Glenmark Pharmaceuticals gets ANDA approval for Norethindrone Acetate and Ethinyl Estradiol Tablets
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.Powered by Capital Market - Live News