美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE"
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
IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE 075588 001 ANDA IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE TABLET;ORAL 200MG;30MG No No 2002/04/08 2002/04/08 CONTRACT PHARMACAL Discontinued
IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE 076478 001 ANDA IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE SUSPENSION;ORAL 100MG/5ML;15MG/5ML No No 2003/11/05 2003/11/05 PERRIGO Discontinued
IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE 077628 001 ANDA IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE TABLET;ORAL 200MG;30MG No No 2006/08/14 2006/08/14 DR REDDYS LABS LTD Over-the-counter
IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE 209235 001 ANDA IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE CAPSULE;ORAL EQ 200MG FREE ACID AND POTASSIUM SALT;30MG No No 2017/12/01 2017/12/01 AUROBINDO PHARMA Over-the-counter
IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE 213565 001 ANDA IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE TABLET;ORAL 200MG;30MG No No 2023/03/10 2023/03/10 AUROBINDO PHARMA LTD Discontinued
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