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
0527-1901-01	0527-1901	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	dexmethylphenidate hydrochloride	TABLET	ORAL	20170925	N/A	ANDA	ANDA209468	Lannett Company, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (0527-1901-01)
0527-1900-01	0527-1900	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20170925	N/A	ANDA	ANDA209468	Lannett Company, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (0527-1900-01)
0527-1899-01	0527-1899	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20170925	N/A	ANDA	ANDA209468	Lannett Company, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (0527-1899-01)