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=ANDA204314"
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
68382-792-30 68382-792 HUMAN PRESCRIPTION DRUG acyclovir acyclovir TABLET ORAL 20140910 N/A ANDA ANDA204314 Zydus Pharmaceuticals (USA) Inc. ACYCLOVIR 800 mg/1 10 BLISTER PACK in 1 CARTON (68382-792-30) / 10 TABLET in 1 BLISTER PACK
68382-791-05 68382-791 HUMAN PRESCRIPTION DRUG acyclovir acyclovir TABLET ORAL 20140910 N/A ANDA ANDA204314 Zydus Pharmaceuticals (USA) Inc. ACYCLOVIR 400 mg/1 500 TABLET in 1 BOTTLE (68382-791-05)
68382-791-06 68382-791 HUMAN PRESCRIPTION DRUG acyclovir acyclovir TABLET ORAL 20140910 N/A ANDA ANDA204314 Zydus Pharmaceuticals (USA) Inc. ACYCLOVIR 400 mg/1 30 TABLET in 1 BOTTLE (68382-791-06)
68382-791-10 68382-791 HUMAN PRESCRIPTION DRUG acyclovir acyclovir TABLET ORAL 20140910 N/A ANDA ANDA204314 Zydus Pharmaceuticals (USA) Inc. ACYCLOVIR 400 mg/1 1000 TABLET in 1 BOTTLE (68382-791-10)
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