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
0406-1810-01	0406-1810	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride Extended-Release	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20150929	N/A	ANDA	ANDA203583	SpecGx LLC	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0406-1810-01)
0406-1820-01	0406-1820	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride Extended-Release	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20150929	N/A	ANDA	ANDA203583	SpecGx LLC	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0406-1820-01)
0406-1830-01	0406-1830	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride Extended-Release	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20150929	N/A	ANDA	ANDA203583	SpecGx LLC	METHYLPHENIDATE HYDROCHLORIDE	30 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0406-1830-01)
0406-1840-01	0406-1840	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride Extended-Release	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20150929	N/A	ANDA	ANDA203583	SpecGx LLC	METHYLPHENIDATE HYDROCHLORIDE	40 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0406-1840-01)
0406-1850-01	0406-1850	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride Extended-Release	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20150929	N/A	ANDA	ANDA203583	SpecGx LLC	METHYLPHENIDATE HYDROCHLORIDE	50 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0406-1850-01)
0406-1860-01	0406-1860	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride Extended-Release	methylphenidate hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20150929	N/A	ANDA	ANDA203583	SpecGx LLC	METHYLPHENIDATE HYDROCHLORIDE	60 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0406-1860-01)