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=ANDA072050"
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
72789-373-01 72789-373 HUMAN PRESCRIPTION DRUG SULINDAC sulindac TABLET ORAL 20240119 N/A ANDA ANDA072050 PD-Rx Pharmaceuticals, Inc. SULINDAC 150 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (72789-373-01)
72789-373-82 72789-373 HUMAN PRESCRIPTION DRUG SULINDAC sulindac TABLET ORAL 20240125 N/A ANDA ANDA072050 PD-Rx Pharmaceuticals, Inc. SULINDAC 150 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (72789-373-82)
53489-478-05 53489-478 HUMAN PRESCRIPTION DRUG SULINDAC sulindac TABLET ORAL 20090904 N/A ANDA ANDA072050 Sun Pharmaceutical Industries, Inc. SULINDAC 150 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (53489-478-05)
53489-478-06 53489-478 HUMAN PRESCRIPTION DRUG SULINDAC sulindac TABLET ORAL 20090904 N/A ANDA ANDA072050 Sun Pharmaceutical Industries, Inc. SULINDAC 150 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (53489-478-06)
53489-478-10 53489-478 HUMAN PRESCRIPTION DRUG SULINDAC sulindac TABLET ORAL 20090904 N/A ANDA ANDA072050 Sun Pharmaceutical Industries, Inc. SULINDAC 150 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (53489-478-10)
53489-478-03 53489-478 HUMAN PRESCRIPTION DRUG SULINDAC sulindac TABLET ORAL 20090904 N/A ANDA ANDA072050 Sun Pharmaceutical Industries, Inc. SULINDAC 150 mg/1 250 TABLET in 1 BOTTLE, PLASTIC (53489-478-03)
53489-478-02 53489-478 HUMAN PRESCRIPTION DRUG SULINDAC sulindac TABLET ORAL 20090904 N/A ANDA ANDA072050 Sun Pharmaceutical Industries, Inc. SULINDAC 150 mg/1 50 TABLET in 1 BOTTLE, PLASTIC (53489-478-02)
53489-478-01 53489-478 HUMAN PRESCRIPTION DRUG SULINDAC sulindac TABLET ORAL 20090904 N/A ANDA ANDA072050 Sun Pharmaceutical Industries, Inc. SULINDAC 150 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (53489-478-01)
0904-7334-60 0904-7334 HUMAN PRESCRIPTION DRUG SULINDAC sulindac TABLET ORAL 20230727 N/A ANDA ANDA072050 Major Pharmaceuticals SULINDAC 150 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (0904-7334-60)
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