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=ANDA071826"
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
68788-8273-3 68788-8273 HUMAN PRESCRIPTION DRUG Minoxidil Minoxidil TABLET ORAL 20221013 N/A ANDA ANDA071826 Preferred Pharmaceuticals Inc. MINOXIDIL 2.5 mg/1 30 TABLET in 1 BOTTLE (68788-8273-3)
72162-1489-1 72162-1489 HUMAN PRESCRIPTION DRUG Minoxidil Minoxidil TABLET ORAL 20231006 N/A ANDA ANDA071826 Bryant Ranch Prepack MINOXIDIL 2.5 mg/1 100 TABLET in 1 BOTTLE (72162-1489-1)
51407-901-01 51407-901 HUMAN PRESCRIPTION DRUG Minoxidil Minoxidil TABLET ORAL 20240711 N/A ANDA ANDA071826 Golden State Medical Supply, Inc. MINOXIDIL 2.5 mg/1 100 TABLET in 1 BOTTLE (51407-901-01)
49884-256-01 49884-256 HUMAN PRESCRIPTION DRUG Minoxidil Minoxidil TABLET ORAL 19881114 N/A ANDA ANDA071826 Endo USA, Inc. MINOXIDIL 2.5 mg/1 100 TABLET in 1 BOTTLE (49884-256-01)
63629-2232-1 63629-2232 HUMAN PRESCRIPTION DRUG Minoxidil Minoxidil TABLET ORAL 20210322 N/A ANDA ANDA071826 Bryant Ranch Prepack MINOXIDIL 2.5 mg/1 100 TABLET in 1 BOTTLE (63629-2232-1)
68084-204-01 68084-204 HUMAN PRESCRIPTION DRUG Minoxidil Minoxidil TABLET ORAL 20070910 N/A ANDA ANDA071826 American Health Packaging MINOXIDIL 2.5 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-204-01) / 1 TABLET in 1 BLISTER PACK (68084-204-11)
63629-9433-1 63629-9433 HUMAN PRESCRIPTION DRUG Minoxidil Minoxidil TABLET ORAL 20221005 N/A ANDA ANDA071826 Bryant Ranch Prepack MINOXIDIL 2.5 mg/1 30 TABLET in 1 BOTTLE (63629-9433-1)
63629-9433-2 63629-9433 HUMAN PRESCRIPTION DRUG Minoxidil Minoxidil TABLET ORAL 20240223 N/A ANDA ANDA071826 Bryant Ranch Prepack MINOXIDIL 2.5 mg/1 90 TABLET in 1 BOTTLE (63629-9433-2)
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