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=ANDA078512"
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
68788-7876-1 68788-7876 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20210308 N/A ANDA ANDA078512 Preferred Pharmaceuticals Inc. ATENOLOL 25 mg/1 100 TABLET in 1 BOTTLE (68788-7876-1)
68788-7876-3 68788-7876 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20210308 N/A ANDA ANDA078512 Preferred Pharmaceuticals Inc. ATENOLOL 25 mg/1 30 TABLET in 1 BOTTLE (68788-7876-3)
68788-7876-6 68788-7876 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20210308 N/A ANDA ANDA078512 Preferred Pharmaceuticals Inc. ATENOLOL 25 mg/1 60 TABLET in 1 BOTTLE (68788-7876-6)
68788-7876-9 68788-7876 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20210308 N/A ANDA ANDA078512 Preferred Pharmaceuticals Inc. ATENOLOL 25 mg/1 90 TABLET in 1 BOTTLE (68788-7876-9)
70518-4099-0 70518-4099 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20240612 N/A ANDA ANDA078512 REMEDYREPACK INC. ATENOLOL 100 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (70518-4099-0)
65862-168-01 65862-168 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20071031 N/A ANDA ANDA078512 Aurobindo Pharma Limited ATENOLOL 25 mg/1 100 TABLET in 1 BOTTLE (65862-168-01)
65862-168-99 65862-168 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20071031 N/A ANDA ANDA078512 Aurobindo Pharma Limited ATENOLOL 25 mg/1 1000 TABLET in 1 BOTTLE (65862-168-99)
65862-169-01 65862-169 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20071031 N/A ANDA ANDA078512 Aurobindo Pharma Limited ATENOLOL 50 mg/1 100 TABLET in 1 BOTTLE (65862-169-01)
65862-169-99 65862-169 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20071031 N/A ANDA ANDA078512 Aurobindo Pharma Limited ATENOLOL 50 mg/1 1000 TABLET in 1 BOTTLE (65862-169-99)
65862-170-01 65862-170 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20071031 N/A ANDA ANDA078512 Aurobindo Pharma Limited ATENOLOL 100 mg/1 100 TABLET in 1 BOTTLE (65862-170-01)
65862-170-99 65862-170 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20071031 N/A ANDA ANDA078512 Aurobindo Pharma Limited ATENOLOL 100 mg/1 1000 TABLET in 1 BOTTLE (65862-170-99)
51655-104-26 51655-104 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20220909 N/A ANDA ANDA078512 Northwind Pharmaceuticals, LLC ATENOLOL 100 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (51655-104-26)
51655-104-52 51655-104 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20231019 N/A ANDA ANDA078512 Northwind Pharmaceuticals, LLC ATENOLOL 100 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-104-52)
0904-7187-61 0904-7187 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20071031 N/A ANDA ANDA078512 Major Pharmaceuticals ATENOLOL 25 mg/1 100 BLISTER PACK in 1 CARTON (0904-7187-61) / 1 TABLET in 1 BLISTER PACK
51655-533-25 51655-533 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20221228 N/A ANDA ANDA078512 Northwind Pharmaceuticals, LLC ATENOLOL 25 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (51655-533-25)
51655-533-26 51655-533 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20221228 N/A ANDA ANDA078512 Northwind Pharmaceuticals, LLC ATENOLOL 25 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (51655-533-26)
51655-533-52 51655-533 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20221228 N/A ANDA ANDA078512 Northwind Pharmaceuticals, LLC ATENOLOL 25 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-533-52)
70518-3036-0 70518-3036 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20210303 N/A ANDA ANDA078512 REMEDYREPACK INC. ATENOLOL 50 mg/1 30 TABLET in 1 BLISTER PACK (70518-3036-0)
70518-3036-1 70518-3036 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20210312 N/A ANDA ANDA078512 REMEDYREPACK INC. ATENOLOL 50 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (70518-3036-1)
70518-3036-3 70518-3036 HUMAN PRESCRIPTION DRUG Atenolol Atenolol TABLET ORAL 20220816 N/A ANDA ANDA078512 REMEDYREPACK INC. ATENOLOL 50 mg/1 30 TABLET in 1 BLISTER PACK (70518-3036-3)
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