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
0078-0441-05	0078-0441	HUMAN PRESCRIPTION DRUG	Ritalin	methylphenidate hydrochloride	TABLET	ORAL	19551231	20260831	NDA	NDA010187	Novartis Pharmaceuticals Corporation	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (0078-0441-05)
0078-0440-05	0078-0440	HUMAN PRESCRIPTION DRUG	Ritalin	methylphenidate hydrochloride	TABLET	ORAL	19551231	20260731	NDA	NDA010187	Novartis Pharmaceuticals Corporation	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (0078-0440-05)
66758-274-01	66758-274	HUMAN PRESCRIPTION DRUG	Ritalin	methylphenidate hydrochloride	TABLET	ORAL	20241218	N/A	NDA	NDA010187	Sandoz Inc	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (66758-274-01)
66758-273-01	66758-273	HUMAN PRESCRIPTION DRUG	Ritalin	methylphenidate hydrochloride	TABLET	ORAL	20250728	N/A	NDA	NDA010187	Sandoz Inc	METHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (66758-273-01)
66758-275-01	66758-275	HUMAN PRESCRIPTION DRUG	Ritalin	methylphenidate hydrochloride	TABLET	ORAL	20241218	N/A	NDA	NDA010187	Sandoz Inc	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (66758-275-01)
0078-0439-05	0078-0439	HUMAN PRESCRIPTION DRUG	Ritalin	methylphenidate hydrochloride	TABLET	ORAL	19551231	20260731	NDA	NDA010187	Novartis Pharmaceuticals Corporation	METHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (0078-0439-05)