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=ANDA212903"
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
72603-278-02 72603-278 HUMAN PRESCRIPTION DRUG Sodium sulfate, potassium sulfate and magnesium sulfate Sodium sulfate, potassium sulfate and magnesium sulfate SOLUTION ORAL 20250301 N/A ANDA ANDA212903 NorthStar RxLLC MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE 1.6 g/177mL; 3.13 g/177mL; 17.5 g/177mL 2 BOTTLE, PLASTIC in 1 CARTON (72603-278-02) / 177 mL in 1 BOTTLE, PLASTIC (72603-278-01)
31722-098-31 31722-098 HUMAN PRESCRIPTION DRUG Sodium sulfate, potassium sulfate and magnesium sulfate Sodium sulfate, potassium sulfate and magnesium sulfate SOLUTION ORAL 20241018 N/A ANDA ANDA212903 Camber Pharmaceuticals, Inc. MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE 1.6 g/177mL; 3.13 g/177mL; 17.5 g/177mL 2 BOTTLE, PLASTIC in 1 CARTON (31722-098-31) / 177 mL in 1 BOTTLE, PLASTIC (31722-098-17)
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