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
62756-200-18	62756-200	HUMAN PRESCRIPTION DRUG	TIAGABINE HYDROCHLORIDE	TIAGABINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20111104	N/A	ANDA	ANDA077555	Sun Pharmaceutical Industries, Inc.	TIAGABINE HYDROCHLORIDE	2 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62756-200-18)
62756-200-83	62756-200	HUMAN PRESCRIPTION DRUG	TIAGABINE HYDROCHLORIDE	TIAGABINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20111104	N/A	ANDA	ANDA077555	Sun Pharmaceutical Industries, Inc.	TIAGABINE HYDROCHLORIDE	2 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62756-200-83)
62756-224-08	62756-224	HUMAN PRESCRIPTION DRUG	TIAGABINE HYDROCHLORIDE	TIAGABINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20111104	N/A	ANDA	ANDA077555	Sun Pharmaceutical Industries, Inc.	TIAGABINE HYDROCHLORIDE	4 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62756-224-08)
62756-224-18	62756-224	HUMAN PRESCRIPTION DRUG	TIAGABINE HYDROCHLORIDE	TIAGABINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20111104	N/A	ANDA	ANDA077555	Sun Pharmaceutical Industries, Inc.	TIAGABINE HYDROCHLORIDE	4 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62756-224-18)
62756-224-83	62756-224	HUMAN PRESCRIPTION DRUG	TIAGABINE HYDROCHLORIDE	TIAGABINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20111104	N/A	ANDA	ANDA077555	Sun Pharmaceutical Industries, Inc.	TIAGABINE HYDROCHLORIDE	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62756-224-83)
62756-224-88	62756-224	HUMAN PRESCRIPTION DRUG	TIAGABINE HYDROCHLORIDE	TIAGABINE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20111104	N/A	ANDA	ANDA077555	Sun Pharmaceutical Industries, Inc.	TIAGABINE HYDROCHLORIDE	4 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62756-224-88)