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）

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
70771-1605-9	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)
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)
70771-1604-9	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)
70771-1604-3	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)
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)
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)