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=ANDA207721"
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
70771-1604-3 70771-1604 HUMAN PRESCRIPTION DRUG Solifenacin Solifenacin TABLET, FILM COATED ORAL 20220210 N/A ANDA ANDA207721 Zydus Lifesciences Limited SOLIFENACIN SUCCINATE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70771-1604-3)
70771-1604-9 70771-1604 HUMAN PRESCRIPTION DRUG Solifenacin Solifenacin TABLET, FILM COATED ORAL 20220210 N/A ANDA ANDA207721 Zydus Lifesciences Limited SOLIFENACIN SUCCINATE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70771-1604-9)
70771-1605-3 70771-1605 HUMAN PRESCRIPTION DRUG Solifenacin Solifenacin TABLET, FILM COATED ORAL 20220210 N/A ANDA ANDA207721 Zydus Lifesciences Limited SOLIFENACIN SUCCINATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70771-1605-3)
70771-1605-9 70771-1605 HUMAN PRESCRIPTION DRUG Solifenacin Solifenacin TABLET, FILM COATED ORAL 20220210 N/A ANDA ANDA207721 Zydus Lifesciences Limited SOLIFENACIN SUCCINATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70771-1605-9)
68382-988-06 68382-988 HUMAN PRESCRIPTION DRUG Solifenacin Solifenacin TABLET, FILM COATED ORAL 20220210 N/A ANDA ANDA207721 Zydus Pharmaceuticals USA Inc. SOLIFENACIN SUCCINATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68382-988-06)
68382-988-16 68382-988 HUMAN PRESCRIPTION DRUG Solifenacin Solifenacin TABLET, FILM COATED ORAL 20220210 N/A ANDA ANDA207721 Zydus Pharmaceuticals USA Inc. SOLIFENACIN SUCCINATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68382-988-16)
68382-987-06 68382-987 HUMAN PRESCRIPTION DRUG Solifenacin Solifenacin TABLET, FILM COATED ORAL 20220210 N/A ANDA ANDA207721 Zydus Pharmaceuticals USA Inc. SOLIFENACIN SUCCINATE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68382-987-06)
68382-987-16 68382-987 HUMAN PRESCRIPTION DRUG Solifenacin Solifenacin TABLET, FILM COATED ORAL 20220210 N/A ANDA ANDA207721 Zydus Pharmaceuticals USA Inc. SOLIFENACIN SUCCINATE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68382-987-16)
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