美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA209366"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
71335-9620-6 71335-9620 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20230419 N/A ANDA ANDA209366 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 60 TABLET in 1 BOTTLE (71335-9620-6)
71335-9620-7 71335-9620 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20230103 N/A ANDA ANDA209366 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 25 TABLET in 1 BOTTLE (71335-9620-7)
71335-9620-8 71335-9620 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20240405 N/A ANDA ANDA209366 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 10 TABLET in 1 BOTTLE (71335-9620-8)
71335-9620-9 71335-9620 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20240405 N/A ANDA ANDA209366 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 40 TABLET in 1 BOTTLE (71335-9620-9)
69452-290-20 69452-290 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20200815 N/A ANDA ANDA209366 Bionpharma Inc. ACYCLOVIR 400 mg/1 100 TABLET in 1 BOTTLE (69452-290-20)
69452-290-30 69452-290 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20200815 N/A ANDA ANDA209366 Bionpharma Inc. ACYCLOVIR 400 mg/1 500 TABLET in 1 BOTTLE (69452-290-30)
69452-291-20 69452-291 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20200815 N/A ANDA ANDA209366 Bionpharma Inc. ACYCLOVIR 800 mg/1 100 TABLET in 1 BOTTLE (69452-291-20)
69452-291-30 69452-291 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20200815 N/A ANDA ANDA209366 Bionpharma Inc. ACYCLOVIR 800 mg/1 500 TABLET in 1 BOTTLE (69452-291-30)
72189-631-14 72189-631 HUMAN PRESCRIPTION DRUG Acyclovir Acyclovir TABLET ORAL 20250626 N/A ANDA ANDA209366 Direct_Rx ACYCLOVIR 400 mg/1 14 TABLET in 1 BOTTLE (72189-631-14)
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