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
69238-1104-3	69238-1104	HUMAN PRESCRIPTION DRUG	Tiagabine Hydrochloride	Tiagabine	TABLET	ORAL	20171208	N/A	ANDA	ANDA208181	Amneal Pharmaceuticals NY LLC	TIAGABINE HYDROCHLORIDE	2 mg/1	30 TABLET in 1 BOTTLE (69238-1104-3)
69238-1106-3	69238-1106	HUMAN PRESCRIPTION DRUG	Tiagabine Hydrochloride	Tiagabine	TABLET	ORAL	20171208	N/A	ANDA	ANDA208181	Amneal Pharmaceuticals NY LLC	TIAGABINE HYDROCHLORIDE	12 mg/1	30 TABLET in 1 BOTTLE (69238-1106-3)
69238-1105-3	69238-1105	HUMAN PRESCRIPTION DRUG	Tiagabine Hydrochloride	Tiagabine	TABLET	ORAL	20171208	N/A	ANDA	ANDA208181	Amneal Pharmaceuticals NY LLC	TIAGABINE HYDROCHLORIDE	4 mg/1	30 TABLET in 1 BOTTLE (69238-1105-3)
69238-1107-3	69238-1107	HUMAN PRESCRIPTION DRUG	Tiagabine Hydrochloride	Tiagabine	TABLET	ORAL	20171208	N/A	ANDA	ANDA208181	Amneal Pharmaceuticals NY LLC	TIAGABINE HYDROCHLORIDE	16 mg/1	30 TABLET in 1 BOTTLE (69238-1107-3)