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=ANDA076438"
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
0406-8320-01 0406-8320 HUMAN PRESCRIPTION DRUG MORPHINE SULFATE MORPHINE SULFATE TABLET, EXTENDED RELEASE ORAL 20030703 N/A ANDA ANDA076438 SpecGx LLC MORPHINE SULFATE 200 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0406-8320-01)
0406-8390-01 0406-8390 HUMAN PRESCRIPTION DRUG MORPHINE SULFATE MORPHINE SULFATE TABLET, EXTENDED RELEASE ORAL 20030703 N/A ANDA ANDA076438 SpecGx LLC MORPHINE SULFATE 100 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0406-8390-01)
0406-8390-23 0406-8390 HUMAN PRESCRIPTION DRUG MORPHINE SULFATE MORPHINE SULFATE TABLET, EXTENDED RELEASE ORAL 20030703 N/A ANDA ANDA076438 SpecGx LLC MORPHINE SULFATE 100 mg/1 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0406-8390-23)
0406-8390-62 0406-8390 HUMAN PRESCRIPTION DRUG MORPHINE SULFATE MORPHINE SULFATE TABLET, EXTENDED RELEASE ORAL 20030703 N/A ANDA ANDA076438 SpecGx LLC MORPHINE SULFATE 100 mg/1 100 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0406-8390-62)
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