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
43386-575-01	43386-575	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20160120	N/A	ANDA	ANDA207884	Lupin Pharmaceuticals,Inc.	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (43386-575-01)
43386-574-01	43386-574	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20160120	N/A	ANDA	ANDA207884	Lupin Pharmaceuticals,Inc.	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (43386-574-01)
43386-573-01	43386-573	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20160120	N/A	ANDA	ANDA207884	Lupin Pharmaceuticals,Inc.	METHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (43386-573-01)