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
69452-121-20	69452-121	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride	Oxybutynin Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200316	N/A	ANDA	ANDA210717	Bionpharma Inc.	OXYBUTYNIN CHLORIDE	15 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69452-121-20)
69452-120-20	69452-120	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride	Oxybutynin Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200316	N/A	ANDA	ANDA210717	Bionpharma Inc.	OXYBUTYNIN CHLORIDE	10 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69452-120-20)
69452-119-20	69452-119	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride	Oxybutynin Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200316	N/A	ANDA	ANDA210717	Bionpharma Inc.	OXYBUTYNIN CHLORIDE	5 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69452-119-20)