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
10702-100-01	10702-100	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20170511	N/A	ANDA	ANDA206932	KVK-TECH, INC.	METHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (10702-100-01)
10702-101-01	10702-101	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20170511	N/A	ANDA	ANDA206932	KVK-TECH, INC.	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (10702-101-01)
10702-102-01	10702-102	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20170511	N/A	ANDA	ANDA206932	KVK-TECH, INC.	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (10702-102-01)