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=ANDA202511"
符合检索条件的记录共 3 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
43386-700-02 43386-700 HUMAN PRESCRIPTION DRUG SODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATE sodium sulfate, potassium sulfate, magnesium sulfate SOLUTION ORAL 20221230 N/A ANDA ANDA202511 Lupin Pharmaceuticals, Inc. MAGNESIUM SULFATE ANHYDROUS; POTASSIUM SULFATE; SODIUM SULFATE 1.6 g/177mL; 3.13 g/177mL; 17.5 g/177mL 1 BOTTLE in 1 CONTAINER (43386-700-02) / 177 mL in 1 BOTTLE
43386-700-83 43386-700 HUMAN PRESCRIPTION DRUG SODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATE sodium sulfate, potassium sulfate, magnesium sulfate SOLUTION ORAL 20221230 N/A ANDA ANDA202511 Lupin Pharmaceuticals, Inc. MAGNESIUM SULFATE ANHYDROUS; POTASSIUM SULFATE; SODIUM SULFATE 1.6 g/177mL; 3.13 g/177mL; 17.5 g/177mL 2 BOTTLE in 1 CARTON (43386-700-83) / 177 mL in 1 BOTTLE
40032-700-83 40032-700 HUMAN PRESCRIPTION DRUG SODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATE sodium sulfate, potassium sulfate, magnesium sulfate SOLUTION ORAL 20170223 N/A ANDA ANDA202511 Novel Laboratories, Inc. MAGNESIUM SULFATE ANHYDROUS; POTASSIUM SULFATE; SODIUM SULFATE 1.6 g/177mL; 3.13 g/177mL; 17.5 g/177mL 2 BOTTLE in 1 CARTON (40032-700-83) / 177 mL in 1 BOTTLE
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