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
0093-5030-56	0093-5030	HUMAN PRESCRIPTION DRUG	Tiagabine Hydrochloride	Tiagabine Hydrochloride	TABLET, FILM COATED	ORAL	20160603	N/A	NDA AUTHORIZED GENERIC	NDA020646	Teva Pharmaceuticals USA, Inc.	TIAGABINE HYDROCHLORIDE	2 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-5030-56)
0093-5031-56	0093-5031	HUMAN PRESCRIPTION DRUG	Tiagabine Hydrochloride	Tiagabine Hydrochloride	TABLET, FILM COATED	ORAL	20160718	N/A	NDA AUTHORIZED GENERIC	NDA020646	Teva Pharmaceuticals USA, Inc.	TIAGABINE HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-5031-56)
0093-8072-56	0093-8072	HUMAN PRESCRIPTION DRUG	Tiagabine Hydrochloride	Tiagabine Hydrochloride	TABLET, FILM COATED	ORAL	20180309	N/A	NDA AUTHORIZED GENERIC	NDA020646	Teva Pharmaceuticals USA, Inc.	TIAGABINE HYDROCHLORIDE	12 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-8072-56)
0093-8076-56	0093-8076	HUMAN PRESCRIPTION DRUG	Tiagabine Hydrochloride	Tiagabine Hydrochloride	TABLET, FILM COATED	ORAL	20180309	N/A	NDA AUTHORIZED GENERIC	NDA020646	Teva Pharmaceuticals USA, Inc.	TIAGABINE HYDROCHLORIDE	16 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-8076-56)