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
57664-083-88	57664-083	HUMAN PRESCRIPTION DRUG	LISDEXAMFETAMINE DIMESYLATE	LISDEXAMFETAMINE DIMESYLATE	TABLET, CHEWABLE	ORAL	20230825	N/A	ANDA	ANDA214134	Sun Pharmaceutical Industries, Inc.	LISDEXAMFETAMINE DIMESYLATE	10 mg/1	100 TABLET, CHEWABLE in 1 BOTTLE (57664-083-88)
57664-087-88	57664-087	HUMAN PRESCRIPTION DRUG	LISDEXAMFETAMINE DIMESYLATE	LISDEXAMFETAMINE DIMESYLATE	TABLET, CHEWABLE	ORAL	20230825	N/A	ANDA	ANDA214134	Sun Pharmaceutical Industries, Inc.	LISDEXAMFETAMINE DIMESYLATE	50 mg/1	100 TABLET, CHEWABLE in 1 BOTTLE (57664-087-88)
57664-086-88	57664-086	HUMAN PRESCRIPTION DRUG	LISDEXAMFETAMINE DIMESYLATE	LISDEXAMFETAMINE DIMESYLATE	TABLET, CHEWABLE	ORAL	20230825	N/A	ANDA	ANDA214134	Sun Pharmaceutical Industries, Inc.	LISDEXAMFETAMINE DIMESYLATE	40 mg/1	100 TABLET, CHEWABLE in 1 BOTTLE (57664-086-88)
57664-088-88	57664-088	HUMAN PRESCRIPTION DRUG	LISDEXAMFETAMINE DIMESYLATE	LISDEXAMFETAMINE DIMESYLATE	TABLET, CHEWABLE	ORAL	20230825	N/A	ANDA	ANDA214134	Sun Pharmaceutical Industries, Inc.	LISDEXAMFETAMINE DIMESYLATE	60 mg/1	100 TABLET, CHEWABLE in 1 BOTTLE (57664-088-88)
57664-084-88	57664-084	HUMAN PRESCRIPTION DRUG	LISDEXAMFETAMINE DIMESYLATE	LISDEXAMFETAMINE DIMESYLATE	TABLET, CHEWABLE	ORAL	20230825	N/A	ANDA	ANDA214134	Sun Pharmaceutical Industries, Inc.	LISDEXAMFETAMINE DIMESYLATE	20 mg/1	100 TABLET, CHEWABLE in 1 BOTTLE (57664-084-88)
57664-085-88	57664-085	HUMAN PRESCRIPTION DRUG	LISDEXAMFETAMINE DIMESYLATE	LISDEXAMFETAMINE DIMESYLATE	TABLET, CHEWABLE	ORAL	20230825	N/A	ANDA	ANDA214134	Sun Pharmaceutical Industries, Inc.	LISDEXAMFETAMINE DIMESYLATE	30 mg/1	100 TABLET, CHEWABLE in 1 BOTTLE (57664-085-88)