美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=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
GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE 214407 002 ANDA GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 1.2GM;120MG No No 2022/02/01 2022/02/01 L PERRIGO CO Over-the-counter
FEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE 215434 001 ANDA FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 60MG;120MG No No 2022/05/31 2022/05/31 DR REDDYS Over-the-counter
NAPROXEN SODIUM AND PSEUDOEPHEDRINE HYDROCHLORIDE 211360 001 ANDA NAPROXEN SODIUM; PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 220MG;120MG No No 2022/06/01 2022/06/01 AUROBINDO PHARMA Over-the-counter
GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE 216082 001 ANDA GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 600MG;60MG No No 2022/08/22 2022/08/22 GRANULES Discontinued
GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE 216082 002 ANDA GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 1.2GM;120MG No No 2022/08/22 2022/08/22 GRANULES Discontinued
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
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
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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