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=ANDA071795"
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
0591-5660-01 0591-5660 HUMAN PRESCRIPTION DRUG Sulindac Sulindac TABLET ORAL 19900403 N/A ANDA ANDA071795 Actavis Pharma, Inc. SULINDAC 200 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01)
0591-5660-05 0591-5660 HUMAN PRESCRIPTION DRUG Sulindac Sulindac TABLET ORAL 19900403 N/A ANDA ANDA071795 Actavis Pharma, Inc. SULINDAC 200 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05)
55289-930-10 55289-930 HUMAN PRESCRIPTION DRUG Sulindac Sulindac TABLET ORAL 20100712 N/A ANDA ANDA071795 PD-Rx Pharmaceuticals, Inc. SULINDAC 200 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10)
55289-930-20 55289-930 HUMAN PRESCRIPTION DRUG Sulindac Sulindac TABLET ORAL 20100712 N/A ANDA ANDA071795 PD-Rx Pharmaceuticals, Inc. SULINDAC 200 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20)
55289-930-30 55289-930 HUMAN PRESCRIPTION DRUG Sulindac Sulindac TABLET ORAL 20100712 N/A ANDA ANDA071795 PD-Rx Pharmaceuticals, Inc. SULINDAC 200 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30)
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