美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=EPHEDRINE 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
LORATADINE AND PSEUDOEPHEDRINE SULFATE 076050 001 ANDA LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE;ORAL 5MG;120MG No No 2003/01/30 2003/01/30 PERRIGO PHARMA INTL Over-the-counter
LORATADINE AND PSEUDOEPHEDRINE SULFATE 075706 001 ANDA LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE;ORAL 10MG;240MG No No 2003/02/21 2003/02/21 P AND L Over-the-counter
LORATADINE AND PSEUDOEPHEDRINE SULFATE 076208 001 ANDA LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE;ORAL 5MG;120MG No No 2004/01/28 2004/01/28 HERITAGE PHARMA Discontinued
LORATADINE AND PSEUDOEPHEDRINE SULFATE 075989 001 ANDA LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE;ORAL 10MG;240MG No No 2004/03/04 2004/03/04 PERRIGO PHARMA INTL Over-the-counter
LORATADINE AND PSEUDOEPHEDRINE SULFATE 076557 001 ANDA LORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE;ORAL 10MG;240MG No No 2004/09/22 2004/09/22 SUN PHARM INDS LTD Over-the-counter
DESLORATADINE AND PSEUDOEPHEDRINE SULFATE 24 HOUR 078366 001 ANDA DESLORATADINE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE;ORAL 5MG;240MG No No 2011/04/26 2011/04/26 DR REDDYS LABS LTD Prescription
DEXBROMPHENIRAMINE MALEATE AND PSEUDOEPHEDRINE SULFATE 078648 001 ANDA DEXBROMPHENIRAMINE MALEATE; PSEUDOEPHEDRINE SULFATE TABLET, EXTENDED RELEASE;ORAL 6MG;120MG No No 2013/02/27 2013/02/27 AVANTHI INC Discontinued
EPHEDRINE SULFATE 208609 001 NDA EPHEDRINE SULFATE SOLUTION;INTRAVENOUS 50MG/ML (50MG/ML) No No 2017/03/01 2017/03/01 AKORN INC Prescription
EPHEDRINE SULFATE 209784 001 ANDA EPHEDRINE SULFATE SOLUTION;INTRAVENOUS 50MG/ML (50MG/ML) No No 2017/08/23 2017/08/23 SANDOZ INC Prescription
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