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
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)
70518-4186-0 70518-4186 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20240925 N/A ANDA ANDA074891 REMEDYREPACK INC. ACYCLOVIR 800 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (70518-4186-0)
70518-2085-1 70518-2085 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20230409 N/A ANDA ANDA074891 REMEDYREPACK INC. ACYCLOVIR 400 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (70518-2085-1)
71205-371-30 71205-371 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20220208 N/A ANDA ANDA074891 Proficient Rx LP ACYCLOVIR 400 mg/1 30 TABLET in 1 BOTTLE (71205-371-30)
71205-371-35 71205-371 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20220208 N/A ANDA ANDA074891 Proficient Rx LP ACYCLOVIR 400 mg/1 35 TABLET in 1 BOTTLE (71205-371-35)
71205-371-60 71205-371 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20220208 N/A ANDA ANDA074891 Proficient Rx LP ACYCLOVIR 400 mg/1 60 TABLET in 1 BOTTLE (71205-371-60)
71205-371-90 71205-371 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20220208 N/A ANDA ANDA074891 Proficient Rx LP ACYCLOVIR 400 mg/1 90 TABLET in 1 BOTTLE (71205-371-90)
71205-388-30 71205-388 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20220208 N/A ANDA ANDA074891 Proficient Rx LP ACYCLOVIR 800 mg/1 30 TABLET in 1 BOTTLE (71205-388-30)
71205-388-35 71205-388 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20220208 N/A ANDA ANDA074891 Proficient Rx LP ACYCLOVIR 800 mg/1 35 TABLET in 1 BOTTLE (71205-388-35)
71205-388-60 71205-388 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20220208 N/A ANDA ANDA074891 Proficient Rx LP ACYCLOVIR 800 mg/1 60 TABLET in 1 BOTTLE (71205-388-60)
71205-388-90 71205-388 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20220208 N/A ANDA ANDA074891 Proficient Rx LP ACYCLOVIR 800 mg/1 90 TABLET in 1 BOTTLE (71205-388-90)
68071-2279-8 68071-2279 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20201015 N/A ANDA ANDA074891 NuCare Pharmaceuticals,Inc. ACYCLOVIR 400 mg/1 15 TABLET in 1 BOTTLE (68071-2279-8)
71335-1645-0 71335-1645 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20200709 N/A ANDA ANDA074891 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 120 TABLET in 1 BOTTLE (71335-1645-0)
71335-1645-1 71335-1645 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20200702 N/A ANDA ANDA074891 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 20 TABLET in 1 BOTTLE (71335-1645-1)
71335-1645-2 71335-1645 HUMAN PRESCRIPTION DRUG ACYCLOVIR ACYCLOVIR TABLET ORAL 20220128 N/A ANDA ANDA074891 Bryant Ranch Prepack ACYCLOVIR 400 mg/1 28 TABLET in 1 BOTTLE (71335-1645-2)
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