美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=DOXEPIN 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
DOXEPIN HYDROCHLORIDE 212357 001 ANDA DOXEPIN HYDROCHLORIDE CREAM;TOPICAL 5% No No 2023/08/16 2023/08/16 AMNEAL Prescription
DOXEPIN HYDROCHLORIDE 217975 001 ANDA DOXEPIN HYDROCHLORIDE CAPSULE;ORAL EQ 10MG BASE No No 2023/08/21 2023/08/21 UNIQUE PHARM Prescription
DOXEPIN HYDROCHLORIDE 217975 002 ANDA DOXEPIN HYDROCHLORIDE CAPSULE;ORAL EQ 25MG BASE No No 2023/08/21 2023/08/21 UNIQUE PHARM Prescription
DOXEPIN HYDROCHLORIDE 217975 003 ANDA DOXEPIN HYDROCHLORIDE CAPSULE;ORAL EQ 50MG BASE No No 2023/08/21 2023/08/21 UNIQUE PHARM Prescription
DOXEPIN HYDROCHLORIDE 217975 004 ANDA DOXEPIN HYDROCHLORIDE CAPSULE;ORAL EQ 75MG BASE No No 2023/08/21 2023/08/21 UNIQUE PHARM Prescription
DOXEPIN HYDROCHLORIDE 217975 005 ANDA DOXEPIN HYDROCHLORIDE CAPSULE;ORAL EQ 100MG BASE No No 2023/08/21 2023/08/21 UNIQUE PHARM Prescription
DOXEPIN HYDROCHLORIDE 218564 001 ANDA DOXEPIN HYDROCHLORIDE TABLET;ORAL EQ 3MG BASE No No 2024/07/01 2024/07/01 AJANTA PHARMA LTD Prescription
DOXEPIN HYDROCHLORIDE 218564 002 ANDA DOXEPIN HYDROCHLORIDE TABLET;ORAL EQ 6MG BASE No No 2024/07/01 2024/07/01 AJANTA PHARMA LTD Prescription
DOXEPIN HYDROCHLORIDE 216041 001 ANDA DOXEPIN HYDROCHLORIDE TABLET;ORAL EQ 3MG BASE No No 2024/07/25 2024/07/25 AUROBINDO PHARMA LTD Discontinued
DOXEPIN HYDROCHLORIDE 216041 002 ANDA DOXEPIN HYDROCHLORIDE TABLET;ORAL EQ 6MG BASE No No 2024/07/25 2024/07/25 AUROBINDO PHARMA LTD Discontinued
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