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
43598-441-01	43598-441	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200820	N/A	ANDA	ANDA213473	Dr.Reddys Laboratories Inc	METHYLPHENIDATE HYDROCHLORIDE	54 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-441-01)
43598-440-01	43598-440	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200820	N/A	ANDA	ANDA213473	Dr.Reddys Laboratories Inc	METHYLPHENIDATE HYDROCHLORIDE	36 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-440-01)
43598-439-01	43598-439	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200820	N/A	ANDA	ANDA213473	Dr.Reddys Laboratories Inc	METHYLPHENIDATE HYDROCHLORIDE	27 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-439-01)
43598-438-01	43598-438	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200820	N/A	ANDA	ANDA213473	Dr.Reddys Laboratories Inc	METHYLPHENIDATE HYDROCHLORIDE	18 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-438-01)