美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=CETIRIZINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE"
符合检索条件的记录共 6 条
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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
CETIRIZINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE 077170 001 ANDA CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 5MG;120MG No No 2008/02/25 2008/02/25 IVAX SUB TEVA PHARMS Over-the-counter
CETIRIZINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE 077991 001 ANDA CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 5MG;120MG No No 2008/03/05 2008/03/05 PLD ACQUISITIONS Over-the-counter
CETIRIZINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE 090922 001 ANDA CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 5MG;120MG No No 2012/09/28 2012/09/28 SUN PHARM INDS LTD Over-the-counter
CETIRIZINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE 210719 001 ANDA CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 5MG;120MG No No 2018/11/16 2018/11/16 PPI-DAC Over-the-counter
CETIRIZINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE 212409 001 ANDA CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 5MG;120MG No No 2023/03/08 2023/03/08 AUROBINDO PHARMA LTD Discontinued
CETIRIZINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE 210507 001 ANDA CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 5MG;120MG No No 2024/09/10 2024/09/10 UNICHEM Over-the-counter
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