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
68682-309-30	68682-309	HUMAN PRESCRIPTION DRUG	budesonide	budesonide	TABLET, EXTENDED RELEASE	ORAL	20180710	N/A	NDA AUTHORIZED GENERIC	NDA203634	Oceanside Pharmaceuticals	BUDESONIDE	9 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-309-30)
68012-309-01	68012-309	HUMAN PRESCRIPTION DRUG	Uceris	budesonide	TABLET, EXTENDED RELEASE	ORAL	20130114	N/A	NDA	NDA203634	Santarus Inc.	BUDESONIDE	9 mg/1	2 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68012-309-01)
68012-309-02	68012-309	HUMAN PRESCRIPTION DRUG	Uceris	budesonide	TABLET, EXTENDED RELEASE	ORAL	20130114	N/A	NDA	NDA203634	Santarus Inc.	BUDESONIDE	9 mg/1	2 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68012-309-02)
68012-309-30	68012-309	HUMAN PRESCRIPTION DRUG	Uceris	budesonide	TABLET, EXTENDED RELEASE	ORAL	20130114	N/A	NDA	NDA203634	Santarus Inc.	BUDESONIDE	9 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68012-309-30)
63629-9093-1	63629-9093	HUMAN PRESCRIPTION DRUG	budesonide	budesonide	TABLET, EXTENDED RELEASE	ORAL	20241030	N/A	NDA AUTHORIZED GENERIC	NDA203634	Bryant Ranch Prepack	BUDESONIDE	9 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-9093-1)