美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=POMALIDOMIDE"
符合检索条件的记录共 32 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
POMALIDOMIDE 210164 001 ANDA POMALIDOMIDE CAPSULE;ORAL 1MG No No 2024/06/11 2024/06/11 APOTEX Prescription
POMALIDOMIDE 210164 002 ANDA POMALIDOMIDE CAPSULE;ORAL 2MG No No 2024/06/11 2024/06/11 APOTEX Prescription
POMALIDOMIDE 210164 003 ANDA POMALIDOMIDE CAPSULE;ORAL 3MG No No 2024/06/11 2024/06/11 APOTEX Prescription
POMALIDOMIDE 210164 004 ANDA POMALIDOMIDE CAPSULE;ORAL 4MG No No 2024/06/11 2024/06/11 APOTEX Prescription
POMALIDOMIDE 210236 001 ANDA POMALIDOMIDE CAPSULE;ORAL 1MG No No 2024/09/26 2024/09/26 HETERO LABS LTD V Prescription
POMALIDOMIDE 210236 002 ANDA POMALIDOMIDE CAPSULE;ORAL 2MG No No 2024/09/26 2024/09/26 HETERO LABS LTD V Prescription
POMALIDOMIDE 210236 003 ANDA POMALIDOMIDE CAPSULE;ORAL 3MG No No 2024/09/26 2024/09/26 HETERO LABS LTD V Prescription
POMALIDOMIDE 210236 004 ANDA POMALIDOMIDE CAPSULE;ORAL 4MG No No 2024/09/26 2024/09/26 HETERO LABS LTD V Prescription
POMALIDOMIDE 210232 001 ANDA POMALIDOMIDE CAPSULE 1MG No No 2026/03/24 (TA) -- SUN PHARMACEUTICAL INDUSTRIES LIMITED None (Tentative Approval)
POMALIDOMIDE 210232 002 ANDA POMALIDOMIDE CAPSULE 2MG No No 2026/03/24 (TA) -- SUN PHARMACEUTICAL INDUSTRIES LIMITED None (Tentative Approval)
POMALIDOMIDE 210232 003 ANDA POMALIDOMIDE CAPSULE 3MG No No 2026/03/24 (TA) -- SUN PHARMACEUTICAL INDUSTRIES LIMITED None (Tentative Approval)
POMALIDOMIDE 210232 004 ANDA POMALIDOMIDE CAPSULE 4MG No No 2026/03/24 (TA) -- SUN PHARMACEUTICAL INDUSTRIES LIMITED None (Tentative Approval)
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