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
63629-8294-1	63629-8294	HUMAN PRESCRIPTION DRUG	Budesonide	Budesonide	CAPSULE, DELAYED RELEASE	ORAL	20200206	N/A	ANDA	ANDA206200	Bryant Ranch Prepack	BUDESONIDE	3 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63629-8294-1)
65162-778-10	65162-778	HUMAN PRESCRIPTION DRUG	Budesonide	Budesonide	CAPSULE, DELAYED RELEASE	ORAL	20170915	N/A	ANDA	ANDA206200	Amneal Pharmaceuticals LLC	BUDESONIDE	3 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65162-778-10)
65162-778-18	65162-778	HUMAN PRESCRIPTION DRUG	Budesonide	Budesonide	CAPSULE, DELAYED RELEASE	ORAL	20170915	N/A	ANDA	ANDA206200	Amneal Pharmaceuticals LLC	BUDESONIDE	3 mg/1	180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65162-778-18)
65162-778-30	65162-778	HUMAN PRESCRIPTION DRUG	Budesonide	Budesonide	CAPSULE, DELAYED RELEASE	ORAL	20170915	N/A	ANDA	ANDA206200	Amneal Pharmaceuticals LLC	BUDESONIDE	3 mg/1	300 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65162-778-30)
65162-778-49	65162-778	HUMAN PRESCRIPTION DRUG	Budesonide	Budesonide	CAPSULE, DELAYED RELEASE	ORAL	20170915	N/A	ANDA	ANDA206200	Amneal Pharmaceuticals LLC	BUDESONIDE	3 mg/1	21 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65162-778-49)