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=ANDA072710"
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
42806-018-01 42806-018 HUMAN PRESCRIPTION DRUG SULINDAC SULINDAC TABLET ORAL 20100125 N/A ANDA ANDA072710 Epic Pharma, LLC SULINDAC 150 mg/1 100 TABLET in 1 BOTTLE (42806-018-01)
42806-018-05 42806-018 HUMAN PRESCRIPTION DRUG SULINDAC SULINDAC TABLET ORAL 20100125 N/A ANDA ANDA072710 Epic Pharma, LLC SULINDAC 150 mg/1 500 TABLET in 1 BOTTLE (42806-018-05)
42806-018-10 42806-018 HUMAN PRESCRIPTION DRUG SULINDAC SULINDAC TABLET ORAL 20100125 N/A ANDA ANDA072710 Epic Pharma, LLC SULINDAC 150 mg/1 1000 TABLET in 1 BOTTLE (42806-018-10)
24658-770-01 24658-770 HUMAN PRESCRIPTION DRUG SULINDAC SULINDAC TABLET ORAL 20161114 N/A ANDA ANDA072710 PuraCap Laboratories LLC dba Blu Pharmaceuticals SULINDAC 150 mg/1 100 TABLET in 1 BOTTLE (24658-770-01)
24658-770-05 24658-770 HUMAN PRESCRIPTION DRUG SULINDAC SULINDAC TABLET ORAL 20161114 N/A ANDA ANDA072710 PuraCap Laboratories LLC dba Blu Pharmaceuticals SULINDAC 150 mg/1 500 TABLET in 1 BOTTLE (24658-770-05)
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