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
57664-228-08	57664-228	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20130816	N/A	ANDA	ANDA090710	Sun Pharmaceutical Industries, Inc.	METHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (57664-228-08)
57664-228-13	57664-228	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20130816	N/A	ANDA	ANDA090710	Sun Pharmaceutical Industries, Inc.	METHYLPHENIDATE HYDROCHLORIDE	5 mg/1	500 TABLET in 1 BOTTLE (57664-228-13)
57664-228-18	57664-228	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20130816	N/A	ANDA	ANDA090710	Sun Pharmaceutical Industries, Inc.	METHYLPHENIDATE HYDROCHLORIDE	5 mg/1	1000 TABLET in 1 BOTTLE (57664-228-18)
57664-228-83	57664-228	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20130816	N/A	ANDA	ANDA090710	Sun Pharmaceutical Industries, Inc.	METHYLPHENIDATE HYDROCHLORIDE	5 mg/1	30 TABLET in 1 BOTTLE (57664-228-83)
57664-228-88	57664-228	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20130816	N/A	ANDA	ANDA090710	Sun Pharmaceutical Industries, Inc.	METHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (57664-228-88)
57664-229-08	57664-229	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20130816	N/A	ANDA	ANDA090710	Sun Pharmaceutical Industries, Inc.	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (57664-229-08)
57664-229-13	57664-229	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20130816	N/A	ANDA	ANDA090710	Sun Pharmaceutical Industries, Inc.	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	500 TABLET in 1 BOTTLE (57664-229-13)
57664-229-18	57664-229	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20130816	N/A	ANDA	ANDA090710	Sun Pharmaceutical Industries, Inc.	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	1000 TABLET in 1 BOTTLE (57664-229-18)
57664-229-83	57664-229	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20130816	N/A	ANDA	ANDA090710	Sun Pharmaceutical Industries, Inc.	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	30 TABLET in 1 BOTTLE (57664-229-83)
57664-229-88	57664-229	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20130816	N/A	ANDA	ANDA090710	Sun Pharmaceutical Industries, Inc.	METHYLPHENIDATE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (57664-229-88)
57664-230-08	57664-230	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20130816	N/A	ANDA	ANDA090710	Sun Pharmaceutical Industries, Inc.	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (57664-230-08)
57664-230-13	57664-230	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20130816	N/A	ANDA	ANDA090710	Sun Pharmaceutical Industries, Inc.	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	500 TABLET in 1 BOTTLE (57664-230-13)
57664-230-18	57664-230	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20130816	N/A	ANDA	ANDA090710	Sun Pharmaceutical Industries, Inc.	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	1000 TABLET in 1 BOTTLE (57664-230-18)
57664-230-83	57664-230	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20130816	N/A	ANDA	ANDA090710	Sun Pharmaceutical Industries, Inc.	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BOTTLE (57664-230-83)
57664-230-88	57664-230	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20130816	N/A	ANDA	ANDA090710	Sun Pharmaceutical Industries, Inc.	METHYLPHENIDATE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (57664-230-88)
63629-1172-1	63629-1172	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20130816	N/A	ANDA	ANDA090710	Bryant Ranch Prepack	METHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (63629-1172-1)
72162-1636-1	72162-1636	HUMAN PRESCRIPTION DRUG	Methylphenidate Hydrochloride	Methylphenidate Hydrochloride	TABLET	ORAL	20240206	N/A	ANDA	ANDA090710	Bryant Ranch Prepack	METHYLPHENIDATE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (72162-1636-1)