美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=PLERIXAFOR"
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
PLERIXAFOR 205182 001 ANDA PLERIXAFOR SOLUTION;SUBCUTANEOUS 24MG/1.2ML (20MG/ML) No No 2023/07/24 2023/07/24 DR REDDYS Prescription
PLERIXAFOR 205197 001 ANDA PLERIXAFOR SOLUTION;SUBCUTANEOUS 24MG/1.2ML (20MG/ML) No No 2023/07/24 2023/07/24 TEVA PHARMS USA INC Prescription
PLERIXAFOR 211901 001 ANDA PLERIXAFOR SOLUTION;SUBCUTANEOUS 24MG/1.2ML (20MG/ML) No No 2023/07/24 2023/07/24 MSN Prescription
PLERIXAFOR 213672 001 ANDA PLERIXAFOR SOLUTION;SUBCUTANEOUS 24MG/1.2ML (20MG/ML) No No 2023/07/24 2023/07/24 EUGIA PHARMA Prescription
PLERIXAFOR 215334 001 ANDA PLERIXAFOR SOLUTION;SUBCUTANEOUS 24MG/1.2ML (20MG/ML) No No 2023/07/24 2023/07/24 AMNEAL Prescription
PLERIXAFOR 215698 001 ANDA PLERIXAFOR SOLUTION;SUBCUTANEOUS 24MG/1.2ML (20MG/ML) No No 2023/07/24 2023/07/24 MEITHEAL Prescription
PLERIXAFOR 208980 001 ANDA PLERIXAFOR SOLUTION;SUBCUTANEOUS 24MG/1.2ML (20MG/ML) No No 2023/07/26 2023/07/26 ZYDUS PHARMS Discontinued
PLERIXAFOR 206644 001 ANDA PLERIXAFOR SOLUTION;SUBCUTANEOUS 24MG/1.2ML (20MG/ML) No No 2024/05/03 2024/05/03 GLAND PHARMA LTD Prescription
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