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
72888-030-01	72888-030	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride	Oxybutynin Chloride	TABLET, EXTENDED RELEASE	ORAL	20201027	N/A	ANDA	ANDA214415	Advagen Pharma Limited	OXYBUTYNIN CHLORIDE	5 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-030-01)
72888-030-05	72888-030	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride	Oxybutynin Chloride	TABLET, EXTENDED RELEASE	ORAL	20240710	N/A	ANDA	ANDA214415	Advagen Pharma Limited	OXYBUTYNIN CHLORIDE	5 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-030-05)
72888-031-01	72888-031	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride	Oxybutynin Chloride	TABLET, EXTENDED RELEASE	ORAL	20201027	N/A	ANDA	ANDA214415	Advagen Pharma Limited	OXYBUTYNIN CHLORIDE	10 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-031-01)
72888-031-05	72888-031	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride	Oxybutynin Chloride	TABLET, EXTENDED RELEASE	ORAL	20240710	N/A	ANDA	ANDA214415	Advagen Pharma Limited	OXYBUTYNIN CHLORIDE	10 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-031-05)
72888-032-01	72888-032	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride	Oxybutynin Chloride	TABLET, EXTENDED RELEASE	ORAL	20201027	N/A	ANDA	ANDA214415	Advagen Pharma Limited	OXYBUTYNIN CHLORIDE	15 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-032-01)
72888-032-05	72888-032	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride	Oxybutynin Chloride	TABLET, EXTENDED RELEASE	ORAL	20240710	N/A	ANDA	ANDA214415	Advagen Pharma Limited	OXYBUTYNIN CHLORIDE	15 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-032-05)