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=ANDA216739"
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
64980-690-01 64980-690 HUMAN PRESCRIPTION DRUG Clomiphene Citrate Clomiphene Citrtae TABLET ORAL 20250915 N/A ANDA ANDA216739 RISING PHARMA HOLDINGS, INC. CLOMIPHENE CITRATE 50 mg/1 10 TABLET in 1 BOTTLE (64980-690-01)
64980-690-03 64980-690 HUMAN PRESCRIPTION DRUG Clomiphene Citrate Clomiphene Citrtae TABLET ORAL 20241119 N/A ANDA ANDA216739 RISING PHARMA HOLDINGS, INC. CLOMIPHENE CITRATE 50 mg/1 30 TABLET in 1 BOTTLE (64980-690-03)
64980-690-90 64980-690 HUMAN PRESCRIPTION DRUG Clomiphene Citrate Clomiphene Citrtae TABLET ORAL 20250915 N/A ANDA ANDA216739 RISING PHARMA HOLDINGS, INC. CLOMIPHENE CITRATE 50 mg/1 1 BLISTER PACK in 1 CARTON (64980-690-90) / 10 TABLET in 1 BLISTER PACK
55801-187-01 55801-187 HUMAN PRESCRIPTION DRUG Clomiphene Citrate Clomiphene Citrtae TABLET ORAL 20241118 N/A ANDA ANDA216739 Appco Pharma LLC CLOMIPHENE CITRATE 50 mg/1 30 TABLET in 1 BOTTLE (55801-187-01)
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