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
57664-379-08	57664-379	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20130926	N/A	ANDA	ANDA201231	Sun Pharmaceutical Industries, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (57664-379-08)
57664-379-13	57664-379	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20130926	N/A	ANDA	ANDA201231	Sun Pharmaceutical Industries, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	500 TABLET in 1 BOTTLE (57664-379-13)
57664-379-18	57664-379	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20130926	N/A	ANDA	ANDA201231	Sun Pharmaceutical Industries, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	1000 TABLET in 1 BOTTLE (57664-379-18)
57664-379-83	57664-379	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20130926	N/A	ANDA	ANDA201231	Sun Pharmaceutical Industries, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	30 TABLET in 1 BOTTLE (57664-379-83)
57664-379-88	57664-379	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20130926	N/A	ANDA	ANDA201231	Sun Pharmaceutical Industries, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (57664-379-88)
57664-378-08	57664-378	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20130926	N/A	ANDA	ANDA201231	Sun Pharmaceutical Industries, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (57664-378-08)
57664-378-13	57664-378	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20130926	N/A	ANDA	ANDA201231	Sun Pharmaceutical Industries, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	500 TABLET in 1 BOTTLE (57664-378-13)
57664-378-18	57664-378	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20130926	N/A	ANDA	ANDA201231	Sun Pharmaceutical Industries, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	1000 TABLET in 1 BOTTLE (57664-378-18)
57664-378-83	57664-378	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20130926	N/A	ANDA	ANDA201231	Sun Pharmaceutical Industries, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	30 TABLET in 1 BOTTLE (57664-378-83)
57664-378-88	57664-378	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20130926	N/A	ANDA	ANDA201231	Sun Pharmaceutical Industries, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (57664-378-88)
57664-376-08	57664-376	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20130926	N/A	ANDA	ANDA201231	Sun Pharmaceutical Industries, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (57664-376-08)
57664-376-13	57664-376	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20130926	N/A	ANDA	ANDA201231	Sun Pharmaceutical Industries, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	2.5 mg/1	500 TABLET in 1 BOTTLE (57664-376-13)
57664-376-18	57664-376	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20130926	N/A	ANDA	ANDA201231	Sun Pharmaceutical Industries, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	2.5 mg/1	1000 TABLET in 1 BOTTLE (57664-376-18)
57664-376-83	57664-376	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20130926	N/A	ANDA	ANDA201231	Sun Pharmaceutical Industries, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	2.5 mg/1	30 TABLET in 1 BOTTLE (57664-376-83)
57664-376-88	57664-376	HUMAN PRESCRIPTION DRUG	Dexmethylphenidate hydrochloride	Dexmethylphenidate hydrochloride	TABLET	ORAL	20130926	N/A	ANDA	ANDA201231	Sun Pharmaceutical Industries, Inc.	DEXMETHYLPHENIDATE HYDROCHLORIDE	2.5 mg/1	100 TABLET in 1 BOTTLE (57664-376-88)