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
0078-0986-15	0078-0986	HUMAN PRESCRIPTION DRUG	MAYZENT	siponimod	TABLET, FILM COATED	ORAL	20190326	N/A	NDA	NDA209884	Novartis Pharmaceuticals Corporation	SIPONIMOD	2 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-0986-15)
0078-0986-45	0078-0986	HUMAN PRESCRIPTION DRUG	MAYZENT	siponimod	TABLET, FILM COATED	ORAL	20220301	N/A	NDA	NDA209884	Novartis Pharmaceuticals Corporation	SIPONIMOD	2 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (0078-0986-45)
0078-0986-93	0078-0986	HUMAN PRESCRIPTION DRUG	MAYZENT	siponimod	TABLET, FILM COATED	ORAL	20190326	N/A	NDA	NDA209884	Novartis Pharmaceuticals Corporation	SIPONIMOD	2 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-0986-93)
0078-0986-94	0078-0986	HUMAN PRESCRIPTION DRUG	MAYZENT	siponimod	TABLET, FILM COATED	ORAL	20220301	N/A	NDA	NDA209884	Novartis Pharmaceuticals Corporation	SIPONIMOD	2 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (0078-0986-94)
0078-1014-15	0078-1014	HUMAN PRESCRIPTION DRUG	MAYZENT	siponimod	TABLET, FILM COATED	ORAL	20220301	N/A	NDA	NDA209884	Novartis Pharmaceuticals Corporation	SIPONIMOD	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-1014-15)
0078-1014-93	0078-1014	HUMAN PRESCRIPTION DRUG	MAYZENT	siponimod	TABLET, FILM COATED	ORAL	20220301	N/A	NDA	NDA209884	Novartis Pharmaceuticals Corporation	SIPONIMOD	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-1014-93)
0078-0979-12	0078-0979	HUMAN PRESCRIPTION DRUG	MAYZENT	siponimod	TABLET, FILM COATED	ORAL	20190326	N/A	NDA	NDA209884	Novartis Pharmaceuticals Corporation	SIPONIMOD	.25 mg/1	12 TABLET, FILM COATED in 1 BLISTER PACK (0078-0979-12)
0078-0979-50	0078-0979	HUMAN PRESCRIPTION DRUG	MAYZENT	siponimod	TABLET, FILM COATED	ORAL	20190326	N/A	NDA	NDA209884	Novartis Pharmaceuticals Corporation	SIPONIMOD	.25 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (0078-0979-50)
0078-0979-89	0078-0979	HUMAN PRESCRIPTION DRUG	MAYZENT	siponimod	TABLET, FILM COATED	ORAL	20220301	N/A	NDA	NDA209884	Novartis Pharmaceuticals Corporation	SIPONIMOD	.25 mg/1	7 TABLET, FILM COATED in 1 BLISTER PACK (0078-0979-89)
0078-0979-92	0078-0979	HUMAN PRESCRIPTION DRUG	MAYZENT	siponimod	TABLET, FILM COATED	ORAL	20190326	N/A	NDA	NDA209884	Novartis Pharmaceuticals Corporation	SIPONIMOD	.25 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (0078-0979-92)