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
57664-336-88	57664-336	HUMAN PRESCRIPTION DRUG	Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate Extended-Release	Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate	CAPSULE, EXTENDED RELEASE	ORAL	20200305	N/A	ANDA	ANDA211715	Sun Pharmaceutical Industries, Inc.	AMPHETAMINE ASPARTATE MONOHYDRATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE	1.25 mg/1; 1.25 mg/1; 1.25 mg/1; 1.25 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (57664-336-88)
57664-337-88	57664-337	HUMAN PRESCRIPTION DRUG	Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate Extended-Release	Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate	CAPSULE, EXTENDED RELEASE	ORAL	20200305	N/A	ANDA	ANDA211715	Sun Pharmaceutical Industries, Inc.	AMPHETAMINE ASPARTATE MONOHYDRATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE	2.5 mg/1; 2.5 mg/1; 2.5 mg/1; 2.5 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (57664-337-88)
57664-338-88	57664-338	HUMAN PRESCRIPTION DRUG	Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate Extended-Release	Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate	CAPSULE, EXTENDED RELEASE	ORAL	20200305	N/A	ANDA	ANDA211715	Sun Pharmaceutical Industries, Inc.	AMPHETAMINE ASPARTATE MONOHYDRATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE	3.75 mg/1; 3.75 mg/1; 3.75 mg/1; 3.75 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (57664-338-88)
57664-339-88	57664-339	HUMAN PRESCRIPTION DRUG	Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate Extended-Release	Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate	CAPSULE, EXTENDED RELEASE	ORAL	20200305	N/A	ANDA	ANDA211715	Sun Pharmaceutical Industries, Inc.	AMPHETAMINE ASPARTATE MONOHYDRATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE	5 mg/1; 5 mg/1; 5 mg/1; 5 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (57664-339-88)
57664-340-88	57664-340	HUMAN PRESCRIPTION DRUG	Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate Extended-Release	Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate	CAPSULE, EXTENDED RELEASE	ORAL	20200305	N/A	ANDA	ANDA211715	Sun Pharmaceutical Industries, Inc.	AMPHETAMINE ASPARTATE MONOHYDRATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE	6.25 mg/1; 6.25 mg/1; 6.25 mg/1; 6.25 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (57664-340-88)
57664-341-88	57664-341	HUMAN PRESCRIPTION DRUG	Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate Extended-Release	Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate	CAPSULE, EXTENDED RELEASE	ORAL	20200305	N/A	ANDA	ANDA211715	Sun Pharmaceutical Industries, Inc.	AMPHETAMINE ASPARTATE MONOHYDRATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE	7.5 mg/1; 7.5 mg/1; 7.5 mg/1; 7.5 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (57664-341-88)