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
10702-076-01	10702-076	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE EXTENDED RELEASE	methylphenidate hydrochloride extended release	TABLET	ORAL	20150609	N/A	ANDA	ANDA207488	KVK-Tech, Inc.	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (10702-076-01)
10702-076-06	10702-076	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE EXTENDED RELEASE	methylphenidate hydrochloride extended release	TABLET	ORAL	20150609	N/A	ANDA	ANDA207488	KVK-Tech, Inc.	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	60 TABLET in 1 BOTTLE (10702-076-06)
10702-075-01	10702-075	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE EXTENDED RELEASE	methylphenidate hydrochloride extended release	TABLET	ORAL	20150609	N/A	ANDA	ANDA207488	KVK-Tech, Inc.	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (10702-075-01)
10702-075-06	10702-075	HUMAN PRESCRIPTION DRUG	METHYLPHENIDATE HYDROCHLORIDE EXTENDED RELEASE	methylphenidate hydrochloride extended release	TABLET	ORAL	20150609	N/A	ANDA	ANDA207488	KVK-Tech, Inc.	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	60 TABLET in 1 BOTTLE (10702-075-06)