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=ANDA090624"
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
70518-2604-5 70518-2604 HUMAN PRESCRIPTION DRUG Sulfamethoxazole and Trimethoprim Sulfamethoxazole and Trimethoprim TABLET ORAL 20220317 N/A ANDA ANDA090624 REMEDYREPACK INC. SULFAMETHOXAZOLE; TRIMETHOPRIM 800 mg/1; 160 mg/1 30 TABLET in 1 BLISTER PACK (70518-2604-5)
70518-2604-6 70518-2604 HUMAN PRESCRIPTION DRUG Sulfamethoxazole and Trimethoprim Sulfamethoxazole and Trimethoprim TABLET ORAL 20220412 N/A ANDA ANDA090624 REMEDYREPACK INC. SULFAMETHOXAZOLE; TRIMETHOPRIM 800 mg/1; 160 mg/1 20 TABLET in 1 BLISTER PACK (70518-2604-6)
70518-2604-7 70518-2604 HUMAN PRESCRIPTION DRUG Sulfamethoxazole and Trimethoprim Sulfamethoxazole and Trimethoprim TABLET ORAL 20220511 N/A ANDA ANDA090624 REMEDYREPACK INC. SULFAMETHOXAZOLE; TRIMETHOPRIM 800 mg/1; 160 mg/1 21 TABLET in 1 BOTTLE, PLASTIC (70518-2604-7)
70518-2604-8 70518-2604 HUMAN PRESCRIPTION DRUG Sulfamethoxazole and Trimethoprim Sulfamethoxazole and Trimethoprim TABLET ORAL 20220527 N/A ANDA ANDA090624 REMEDYREPACK INC. SULFAMETHOXAZOLE; TRIMETHOPRIM 800 mg/1; 160 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (70518-2604-8)
70518-2604-9 70518-2604 HUMAN PRESCRIPTION DRUG Sulfamethoxazole and Trimethoprim Sulfamethoxazole and Trimethoprim TABLET ORAL 20220607 N/A ANDA ANDA090624 REMEDYREPACK INC. SULFAMETHOXAZOLE; TRIMETHOPRIM 800 mg/1; 160 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (70518-2604-9)
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