美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=ACYCLOVIR"
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
ACYCLOVIR 212444 001 ANDA ACYCLOVIR OINTMENT;TOPICAL 5% No No 2021/05/19 2021/05/19 MACLEODS PHARMS LTD Prescription
ACYCLOVIR 212202 001 ANDA ACYCLOVIR OINTMENT;TOPICAL 5% No No 2021/11/15 2021/11/15 PRINSTON INC Discontinued
ACYCLOVIR 216331 001 ANDA ACYCLOVIR SUSPENSION;ORAL 200MG/5ML No No 2022/03/31 2022/03/31 AUROBINDO PHARMA Prescription
ACYCLOVIR 215669 001 ANDA ACYCLOVIR SUSPENSION;ORAL 200MG/5ML No No 2022/07/01 2022/07/01 HETERO LABS LTD III Prescription
ACYCLOVIR 215724 001 ANDA ACYCLOVIR SUSPENSION;ORAL 200MG/5ML No No 2022/08/18 2022/08/18 RUBICON Prescription
ACYCLOVIR 206770 001 ANDA ACYCLOVIR CREAM;TOPICAL 5% No No 2023/02/28 2023/02/28 ZYDUS LIFESCIENCES Prescription
ACYCLOVIR 217393 001 ANDA ACYCLOVIR SUSPENSION;ORAL 200MG/5ML No No 2023/03/09 2023/03/09 MSN Prescription
ACYCLOVIR 212361 001 ANDA ACYCLOVIR CREAM;TOPICAL 5% No No 2023/11/21 2023/11/21 ALEMBIC Prescription
ACYCLOVIR SODIUM 218111 001 ANDA ACYCLOVIR SODIUM INJECTABLE;INJECTION EQ 50MG BASE/ML No No 2024/01/08 2024/01/08 SLATE RUN PHARMA Prescription
ACYCLOVIR 205470 001 ANDA ACYCLOVIR CREAM;TOPICAL 5% No No 2024/06/12 2024/06/12 TARO Prescription
ACYCLOVIR SODIUM 215404 001 ANDA ACYCLOVIR SODIUM INJECTABLE;INJECTION EQ 50MG BASE/ML No No 2024/06/25 2024/06/25 FRESENIUS KABI USA Prescription
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