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=ANDA075500"
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
72162-2583-1 72162-2583 HUMAN PRESCRIPTION DRUG SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET ORAL 20251124 N/A ANDA ANDA075500 Bryant Ranch Prepack SOTALOL HYDROCHLORIDE 80 mg/1 100 TABLET in 1 BOTTLE (72162-2583-1)
11788-054-01 11788-054 HUMAN PRESCRIPTION DRUG SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET ORAL 20251101 N/A ANDA ANDA075500 AiPing Pharmaceutical, Inc. SOTALOL HYDROCHLORIDE 240 mg/1 100 TABLET in 1 BOTTLE (11788-054-01)
72162-2585-1 72162-2585 HUMAN PRESCRIPTION DRUG SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET ORAL 20251124 N/A ANDA ANDA075500 Bryant Ranch Prepack SOTALOL HYDROCHLORIDE 160 mg/1 100 TABLET in 1 BOTTLE (72162-2585-1)
11788-052-01 11788-052 HUMAN PRESCRIPTION DRUG SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET ORAL 20251101 N/A ANDA ANDA075500 AiPing Pharmaceutical, Inc. SOTALOL HYDROCHLORIDE 120 mg/1 100 TABLET in 1 BOTTLE (11788-052-01)
72162-2584-1 72162-2584 HUMAN PRESCRIPTION DRUG SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET ORAL 20251124 N/A ANDA ANDA075500 Bryant Ranch Prepack SOTALOL HYDROCHLORIDE 120 mg/1 100 TABLET in 1 BOTTLE (72162-2584-1)
11788-051-01 11788-051 HUMAN PRESCRIPTION DRUG SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET ORAL 20251101 N/A ANDA ANDA075500 AiPing Pharmaceutical, Inc. SOTALOL HYDROCHLORIDE 80 mg/1 100 TABLET in 1 BOTTLE (11788-051-01)
72162-2586-1 72162-2586 HUMAN PRESCRIPTION DRUG SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET ORAL 20251124 N/A ANDA ANDA075500 Bryant Ranch Prepack SOTALOL HYDROCHLORIDE 240 mg/1 100 TABLET in 1 BOTTLE (72162-2586-1)
11788-053-01 11788-053 HUMAN PRESCRIPTION DRUG SOTALOL HYDROCHLORIDE SOTALOL HYDROCHLORIDE TABLET ORAL 20251101 N/A ANDA ANDA075500 AiPing Pharmaceutical, Inc. SOTALOL HYDROCHLORIDE 160 mg/1 100 TABLET in 1 BOTTLE (11788-053-01)
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