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
0115-1738-01	0115-1738	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20160920	N/A	ANDA	ANDA205105	Amneal Pharmaceuticals of New York LLC	METHYLPHENIDATE HYDROCHLORIDE	30 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0115-1738-01)
0115-1739-01	0115-1739	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20160920	N/A	ANDA	ANDA205105	Amneal Pharmaceuticals of New York LLC	METHYLPHENIDATE HYDROCHLORIDE	40 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0115-1739-01)
0115-1740-01	0115-1740	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20160920	N/A	ANDA	ANDA205105	Amneal Pharmaceuticals of New York LLC	METHYLPHENIDATE HYDROCHLORIDE	50 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0115-1740-01)
0115-1741-01	0115-1741	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20160920	N/A	ANDA	ANDA205105	Amneal Pharmaceuticals of New York LLC	METHYLPHENIDATE HYDROCHLORIDE	60 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0115-1741-01)
0115-1737-01	0115-1737	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20160920	N/A	ANDA	ANDA205105	Amneal Pharmaceuticals of New York LLC	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0115-1737-01)
0115-1736-01	0115-1736	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20160920	N/A	ANDA	ANDA205105	Amneal Pharmaceuticals of New York LLC	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0115-1736-01)