美国FDA药品橙皮书数据库
（U.S. FDA Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations）
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数据记录共 47588 条，共 2380 页，当前第 4 页
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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 是否参比药物 是否生物等效参考标准 治疗等效代码 产品批准日期 申请人 市场状态 专利及市场独占权
TRIHEXYPHENIDYL HYDROCHLORIDE 040184 001 ANDA TRIHEXYPHENIDYL HYDROCHLORIDE TABLET;ORAL 2MG No No 1998/02/06 WATSON LABS DISCN 详细信息
TRIHEXYPHENIDYL HYDROCHLORIDE 084363 001 ANDA TRIHEXYPHENIDYL HYDROCHLORIDE TABLET;ORAL 2MG No Yes AA Approved Prior to Jan 1, 1982 WATSON LABS RX 详细信息
TRIHEXYPHENIDYL HYDROCHLORIDE 085117 001 ANDA TRIHEXYPHENIDYL HYDROCHLORIDE TABLET;ORAL 2MG No No Approved Prior to Jan 1, 1982 WATSON LABS DISCN 详细信息
TRIHEXYPHENIDYL HYDROCHLORIDE 040184 002 ANDA TRIHEXYPHENIDYL HYDROCHLORIDE TABLET;ORAL 5MG No No 1998/02/06 WATSON LABS DISCN 详细信息
TRIHEXYPHENIDYL HYDROCHLORIDE 084364 001 ANDA TRIHEXYPHENIDYL HYDROCHLORIDE TABLET;ORAL 5MG No Yes AA Approved Prior to Jan 1, 1982 WATSON LABS RX 详细信息
TRIHEXYPHENIDYL HYDROCHLORIDE 085105 001 ANDA TRIHEXYPHENIDYL HYDROCHLORIDE TABLET;ORAL 5MG No No Approved Prior to Jan 1, 1982 WATSON LABS DISCN 详细信息
TRIKAFTA (COPACKAGED) 212273 002 NDA ELEXACAFTOR, IVACAFTOR, TEZACAFTOR; IVACAFTOR TABLET;ORAL 50MG,37.5MG,25MG; 75MG Yes No 2021/06/08 VERTEX PHARMS INC RX 详细信息
TRIKAFTA (COPACKAGED) 212273 001 NDA ELEXACAFTOR, IVACAFTOR, TEZACAFTOR; IVACAFTOR TABLET;ORAL 100MG,75MG,50MG; 150MG Yes Yes 2019/10/21 VERTEX PHARMS INC RX 详细信息
TRILAFON 010775 001 NDA PERPHENAZINE TABLET;ORAL 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No Approved Prior to Jan 1, 1982 SCHERING DISCN 详细信息
TRILAFON 010775 002 NDA PERPHENAZINE TABLET;ORAL 4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No Approved Prior to Jan 1, 1982 SCHERING DISCN 详细信息
TRILAFON 010775 003 NDA PERPHENAZINE TABLET;ORAL 8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No Approved Prior to Jan 1, 1982 SCHERING DISCN 详细信息
TRILAFON 010775 004 NDA PERPHENAZINE TABLET;ORAL 16MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No Approved Prior to Jan 1, 1982 SCHERING DISCN 详细信息
TRILEPTAL 021014 001 NDA OXCARBAZEPINE TABLET;ORAL 150MG Yes No AB 2000/01/14 NOVARTIS RX 详细信息
TRILEPTAL 021014 002 NDA OXCARBAZEPINE TABLET;ORAL 300MG Yes No AB 2000/01/14 NOVARTIS RX 详细信息
TRILEPTAL 021014 003 NDA OXCARBAZEPINE TABLET;ORAL 600MG Yes Yes AB 2000/01/14 NOVARTIS RX 详细信息
TRILITRON 088515 001 ANDA PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE TABLET;ORAL 60MG;2.5MG No No 1985/01/09 NEWTRON PHARMS DISCN 详细信息
TRIMETHOPRIM 018679 001 NDA TRIMETHOPRIM TABLET;ORAL 100MG Yes Yes AB 1982/07/30 DR REDDYS LABS SA RX 详细信息
TRIMETHOPRIM 091437 001 ANDA TRIMETHOPRIM TABLET;ORAL 100MG No No AB 2011/06/15 NOVEL LABS INC RX 详细信息
TRIMETHOPRIM 216393 001 ANDA TRIMETHOPRIM TABLET;ORAL 100MG No No AB 2022/10/28 NOVITIUM PHARMA RX 详细信息
TRIMETHOPRIM 070494 001 ANDA TRIMETHOPRIM TABLET;ORAL 100MG No No 1986/01/22 SUN PHARM INDUSTRIES DISCN 详细信息
当前数据更新日期：2026年01月14日，更多信息请点击此处查询美国FDA药品数据库
数据库说明：本数据与美国FDA官方药品橙皮书数据库同步，在官方数据基础上，提供更全面的检索方式和更简洁高效、完整的数据展现，并且可以回溯专利及市场独占权（市场排他数据）历史信息。
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