美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA076380"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
51285-131-97 51285-131 HUMAN PRESCRIPTION DRUG Loestrin 21 Day Norethindrone Acetate and Ethinyl Estradiol TABLET ORAL 20150226 N/A ANDA ANDA076380 Teva Women's Health LLC ETHINYL ESTRADIOL; NORETHINDRONE ACETATE 20 ug/1; 1 mg/1 5 POUCH in 1 CARTON (51285-131-97) / 1 BLISTER PACK in 1 POUCH / 21 TABLET in 1 BLISTER PACK
67296-1159-1 67296-1159 HUMAN PRESCRIPTION DRUG Junel 21 Day Norethindrone Acetate and Ethinyl Estradiol TABLET ORAL 20030918 N/A ANDA ANDA076380 RedPharm Drug ETHINYL ESTRADIOL; NORETHINDRONE ACETATE 20 ug/1; 1 mg/1 28 TABLET in 1 CARTON (67296-1159-1)
82804-172-21 82804-172 HUMAN PRESCRIPTION DRUG Junel 21 Day Norethindrone Acetate and Ethinyl Estradiol TABLET ORAL 20241206 N/A ANDA ANDA076380 Proficient Rx LP ETHINYL ESTRADIOL; NORETHINDRONE ACETATE 20 ug/1; 1 mg/1 3 POUCH in 1 CARTON (82804-172-21) / 1 BLISTER PACK in 1 POUCH / 21 TABLET in 1 BLISTER PACK
72189-215-28 72189-215 HUMAN PRESCRIPTION DRUG Junel FE Junel FE TABLET ORAL 20211006 N/A ANDA ANDA076380 Direct_Rx ETHINYL ESTRADIOL; NORETHINDRONE ACETATE 20 ug/1; 1 mg/1 28 TABLET in 1 POUCH (72189-215-28)
0555-9025-42 0555-9025 HUMAN PRESCRIPTION DRUG Junel 21 Day Norethindrone Acetate and Ethinyl Estradiol TABLET ORAL 20030918 N/A ANDA ANDA076380 Teva Pharmaceuticals USA, Inc. ETHINYL ESTRADIOL; NORETHINDRONE ACETATE 20 ug/1; 1 mg/1 3 POUCH in 1 CARTON (0555-9025-42) / 1 BLISTER PACK in 1 POUCH / 21 TABLET in 1 BLISTER PACK
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