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
0078-0512-05	0078-0512	HUMAN PRESCRIPTION DRUG	Tegretol XR	carbamazepine	TABLET, EXTENDED RELEASE	ORAL	19960325	N/A	NDA	NDA020234	Novartis Pharmaceuticals Corporation	CARBAMAZEPINE	400 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0078-0512-05)
0078-0511-05	0078-0511	HUMAN PRESCRIPTION DRUG	Tegretol XR	carbamazepine	TABLET, EXTENDED RELEASE	ORAL	19960325	N/A	NDA	NDA020234	Novartis Pharmaceuticals Corporation	CARBAMAZEPINE	200 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0078-0511-05)
0781-8016-01	0781-8016	HUMAN PRESCRIPTION DRUG	Carbamazepine ER	Carbamazepine	TABLET, EXTENDED RELEASE	ORAL	20180109	N/A	NDA AUTHORIZED GENERIC	NDA020234	Sandoz Inc	CARBAMAZEPINE	100 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-8016-01)
0078-0510-05	0078-0510	HUMAN PRESCRIPTION DRUG	Tegretol XR	carbamazepine	TABLET, EXTENDED RELEASE	ORAL	19960325	N/A	NDA	NDA020234	Novartis Pharmaceuticals Corporation	CARBAMAZEPINE	100 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0078-0510-05)
0781-5987-01	0781-5987	HUMAN PRESCRIPTION DRUG	Carbamazepine ER	Carbamazepine	TABLET, EXTENDED RELEASE	ORAL	19960325	N/A	NDA AUTHORIZED GENERIC	NDA020234	Sandoz Inc	CARBAMAZEPINE	200 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5987-01)
0781-5988-01	0781-5988	HUMAN PRESCRIPTION DRUG	Carbamazepine ER	Carbamazepine	TABLET, EXTENDED RELEASE	ORAL	19960325	N/A	NDA AUTHORIZED GENERIC	NDA020234	Sandoz Inc	CARBAMAZEPINE	400 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5988-01)