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）
检索条件:" 注册申请号=ANDA076353"
符合检索条件的记录共 3 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
0406-8962-01 0406-8962 HUMAN PRESCRIPTION DRUG Dextroamphetamine Sulfate Extended-Release dextroamphetamine sulfate CAPSULE, EXTENDED RELEASE ORAL 20030506 N/A ANDA ANDA076353 SpecGx LLC DEXTROAMPHETAMINE SULFATE 15 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0406-8962-01)
0406-8960-01 0406-8960 HUMAN PRESCRIPTION DRUG Dextroamphetamine Sulfate Extended-Release dextroamphetamine sulfate CAPSULE, EXTENDED RELEASE ORAL 20030506 N/A ANDA ANDA076353 SpecGx LLC DEXTROAMPHETAMINE SULFATE 5 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0406-8960-01)
0406-8961-01 0406-8961 HUMAN PRESCRIPTION DRUG Dextroamphetamine Sulfate Extended-Release dextroamphetamine sulfate CAPSULE, EXTENDED RELEASE ORAL 20030506 N/A ANDA ANDA076353 SpecGx LLC DEXTROAMPHETAMINE SULFATE 10 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0406-8961-01)
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