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=ANDA076900"
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
65841-023-24 65841-023 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20051008 N/A ANDA ANDA076900 Zydus Lifesciences Limited ATENOLOL 50 mg/1 10000 TABLET in 1 BOTTLE (65841-023-24)
65841-023-40 65841-023 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20051008 N/A ANDA ANDA076900 Zydus Lifesciences Limited ATENOLOL 50 mg/1 5000 TABLET in 1 BOTTLE (65841-023-40)
65841-023-01 65841-023 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20051008 N/A ANDA ANDA076900 Zydus Lifesciences Limited ATENOLOL 50 mg/1 100 TABLET in 1 BOTTLE (65841-023-01)
65841-023-02 65841-023 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20051008 N/A ANDA ANDA076900 Zydus Lifesciences Limited ATENOLOL 50 mg/1 2000 TABLET in 1 BOTTLE (65841-023-02)
65841-023-10 65841-023 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20051008 N/A ANDA ANDA076900 Zydus Lifesciences Limited ATENOLOL 50 mg/1 1000 TABLET in 1 BOTTLE (65841-023-10)
72789-144-30 72789-144 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20201111 N/A ANDA ANDA076900 PD-Rx Pharmaceuticals, Inc. ATENOLOL 50 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (72789-144-30)
72789-144-90 72789-144 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20201030 N/A ANDA ANDA076900 PD-Rx Pharmaceuticals, Inc. ATENOLOL 50 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (72789-144-90)
43063-952-30 43063-952 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20201018 N/A ANDA ANDA076900 PD-Rx Pharmaceuticals, Inc. ATENOLOL 25 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (43063-952-30)
43063-952-90 43063-952 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20190228 N/A ANDA ANDA076900 PD-Rx Pharmaceuticals, Inc. ATENOLOL 25 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (43063-952-90)
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