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
68788-7210-8	68788-7210	HUMAN PRESCRIPTION DRUG	CARBAMAZEPINE	CARBAMAZEPINE	TABLET	ORAL	20180806	N/A	ANDA	ANDA075948	Preferred Pharmaceuticals Inc.	CARBAMAZEPINE	200 mg/1	28 TABLET in 1 BOTTLE (68788-7210-8)
68788-7210-9	68788-7210	HUMAN PRESCRIPTION DRUG	CARBAMAZEPINE	CARBAMAZEPINE	TABLET	ORAL	20180806	N/A	ANDA	ANDA075948	Preferred Pharmaceuticals Inc.	CARBAMAZEPINE	200 mg/1	90 TABLET in 1 BOTTLE (68788-7210-9)
72162-1708-1	72162-1708	HUMAN PRESCRIPTION DRUG	CARBAMAZEPINE	CARBAMAZEPINE	TABLET	ORAL	20250512	N/A	ANDA	ANDA075948	Bryant Ranch Prepack	CARBAMAZEPINE	200 mg/1	100 TABLET in 1 BOTTLE (72162-1708-1)
60505-0183-0	60505-0183	HUMAN PRESCRIPTION DRUG	CARBAMAZEPINE	CARBAMAZEPINE	TABLET	ORAL	20020901	N/A	ANDA	ANDA075948	Apotex Corp.	CARBAMAZEPINE	200 mg/1	100 TABLET in 1 BOTTLE (60505-0183-0)
60505-0183-1	60505-0183	HUMAN PRESCRIPTION DRUG	CARBAMAZEPINE	CARBAMAZEPINE	TABLET	ORAL	20020901	N/A	ANDA	ANDA075948	Apotex Corp.	CARBAMAZEPINE	200 mg/1	1000 TABLET in 1 BOTTLE (60505-0183-1)