美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE 202511 001 ANDA MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE SOLUTION;ORAL 1.6GM/BOT;3.13GM/BOT;17.5GM/BOT No No 2017/02/23 2017/02/23 NOVEL LABS INC Prescription
SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE 215469 001 ANDA MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE SOLUTION;ORAL 1.6GM/BOT;3.13GM/BOT;17.5GM/BOT No No 2023/11/22 2023/11/22 STRIDES PHARMA Prescription
SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE 213924 001 ANDA MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE SOLUTION;ORAL 1.6GM/BOT;3.13GM/BOT;17.5GM/BOT No No 2023/12/29 2023/12/29 ALKEM LABS LTD Prescription
SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE 206431 001 ANDA MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE SOLUTION;ORAL 1.6GM/BOT;3.13GM/BOT;17.5GM/BOT No No 2024/03/19 2024/03/19 TARO Prescription
SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE 204135 001 ANDA MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE SOLUTION;ORAL 1.6GM/BOT;3.13GM/BOT;17.5GM/BOT No No 2024/06/24 2024/06/24 BIONPHARMA Prescription
SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE 209941 001 ANDA MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE SOLUTION;ORAL 1.6GM/BOT;3.13GM/BOT;17.5GM/BOT No No 2024/07/15 2024/07/15 PAI HOLDINGS Prescription
SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE 212903 001 ANDA MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE SOLUTION;ORAL 1.6GM/BOT;3.13GM/BOT;17.5GM/BOT No No 2024/10/18 2024/10/18 ANNORA PHARMA Prescription
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