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
43386-860-01	43386-860	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20151204	N/A	ANDA	ANDA204534	Lupin Pharmaceuticals,Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (43386-860-01)
43386-861-01	43386-861	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20151204	N/A	ANDA	ANDA204534	Lupin Pharmaceuticals,Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (43386-861-01)
43386-862-01	43386-862	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate Hydrochloride	Dexmethylphenidate Hydrochloride	TABLET	ORAL	20151204	N/A	ANDA	ANDA204534	Lupin Pharmaceuticals,Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (43386-862-01)