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
0078-1098-94	0078-1098	HUMAN PRESCRIPTION DRUG	SCEMBLIX	asciminib	TABLET, FILM COATED	ORAL	20211029	N/A	NDA	NDA215358	Novartis Pharmaceuticals Corporation	ASCIMINIB HYDROCHLORIDE	40 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (0078-1098-94)
0078-1098-20	0078-1098	HUMAN PRESCRIPTION DRUG	SCEMBLIX	asciminib	TABLET, FILM COATED	ORAL	20211029	N/A	NDA	NDA215358	Novartis Pharmaceuticals Corporation	ASCIMINIB HYDROCHLORIDE	40 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (0078-1098-20)
0078-1091-94	0078-1091	HUMAN PRESCRIPTION DRUG	SCEMBLIX	asciminib	TABLET, FILM COATED	ORAL	20211029	N/A	NDA	NDA215358	Novartis Pharmaceuticals Corporation	ASCIMINIB HYDROCHLORIDE	20 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (0078-1091-94)
0078-1091-20	0078-1091	HUMAN PRESCRIPTION DRUG	SCEMBLIX	asciminib	TABLET, FILM COATED	ORAL	20211029	N/A	NDA	NDA215358	Novartis Pharmaceuticals Corporation	ASCIMINIB HYDROCHLORIDE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (0078-1091-20)
0078-1196-20	0078-1196	HUMAN PRESCRIPTION DRUG	SCEMBLIX	asciminib	TABLET, FILM COATED	ORAL	20240418	N/A	NDA	NDA215358	Novartis Pharmaceuticals Corporation	ASCIMINIB HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (0078-1196-20)