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=ANDA074891"
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
71335-1645-7 71335-1645 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20201218 N/A ANDA ANDA074891 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 25 TABLET in 1 BOTTLE (71335-1645-7)
71335-1645-8 71335-1645 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20201223 N/A ANDA ANDA074891 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 10 TABLET in 1 BOTTLE (71335-1645-8)
71335-1645-9 71335-1645 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20220128 N/A ANDA ANDA074891 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 40 TABLET in 1 BOTTLE (71335-1645-9)
23155-227-01 23155-227 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20130808 N/A ANDA ANDA074891 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. ACYCLOVIR 400 mg/1 100 TABLET in 1 BOTTLE (23155-227-01)
23155-227-05 23155-227 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20130808 N/A ANDA ANDA074891 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. ACYCLOVIR 400 mg/1 500 TABLET in 1 BOTTLE (23155-227-05)
23155-228-01 23155-228 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20130808 N/A ANDA ANDA074891 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. ACYCLOVIR 800 mg/1 100 TABLET in 1 BOTTLE (23155-228-01)
23155-228-05 23155-228 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20130808 N/A ANDA ANDA074891 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. ACYCLOVIR 800 mg/1 500 TABLET in 1 BOTTLE (23155-228-05)
71335-1757-1 71335-1757 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20220128 N/A ANDA ANDA074891 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 35 TABLET in 1 BOTTLE (71335-1757-1)
71335-1757-2 71335-1757 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20210104 N/A ANDA ANDA074891 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 90 TABLET in 1 BOTTLE (71335-1757-2)
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