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
67877-616-01	67877-616	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20191006	N/A	ANDA	ANDA211779	Ascend Laboratories, LLC	METHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (67877-616-01)
67877-616-33	67877-616	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20191006	N/A	ANDA	ANDA211779	Ascend Laboratories, LLC	METHYLPHENIDATE HYDROCHLORIDE	5 mg/1	10 BLISTER PACK in 1 CARTON (67877-616-33) / 1 TABLET in 1 BLISTER PACK
67877-617-01	67877-617	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20191006	N/A	ANDA	ANDA211779	Ascend Laboratories, LLC	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (67877-617-01)
67877-617-33	67877-617	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20191006	N/A	ANDA	ANDA211779	Ascend Laboratories, LLC	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	10 BLISTER PACK in 1 CARTON (67877-617-33) / 1 TABLET in 1 BLISTER PACK
67877-618-01	67877-618	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20191006	N/A	ANDA	ANDA211779	Ascend Laboratories, LLC	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (67877-618-01)
67877-618-33	67877-618	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20191006	N/A	ANDA	ANDA211779	Ascend Laboratories, LLC	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	10 BLISTER PACK in 1 CARTON (67877-618-33) / 1 TABLET in 1 BLISTER PACK