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=ANDA208701"
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
72241-024-05 72241-024 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20210823 N/A ANDA ANDA208701 Modavar Pharmaceuticals LLC CELECOXIB 200 mg/1 100 CAPSULE in 1 BOTTLE (72241-024-05)
72241-024-10 72241-024 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20210823 N/A ANDA ANDA208701 Modavar Pharmaceuticals LLC CELECOXIB 200 mg/1 500 CAPSULE in 1 BOTTLE (72241-024-10)
72241-024-11 72241-024 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20210823 N/A ANDA ANDA208701 Modavar Pharmaceuticals LLC CELECOXIB 200 mg/1 1000 CAPSULE in 1 BOTTLE (72241-024-11)
72241-025-03 72241-025 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20210823 N/A ANDA ANDA208701 Modavar Pharmaceuticals LLC CELECOXIB 400 mg/1 60 CAPSULE in 1 BOTTLE (72241-025-03)
72241-025-20 72241-025 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20210823 N/A ANDA ANDA208701 Modavar Pharmaceuticals LLC CELECOXIB 400 mg/1 600 CAPSULE in 1 BOTTLE (72241-025-20)
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