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=ANDA219494"
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
64980-706-01 64980-706 HUMAN PRESCRIPTION DRUG Spironolactone Spironolactone TABLET ORAL 20250915 N/A ANDA ANDA219494 Rising Pharma Holdings, Inc. SPIRONOLACTONE 25 mg/1 100 TABLET in 1 BOTTLE (64980-706-01)
64980-706-50 64980-706 HUMAN PRESCRIPTION DRUG Spironolactone Spironolactone TABLET ORAL 20250915 N/A ANDA ANDA219494 Rising Pharma Holdings, Inc. SPIRONOLACTONE 25 mg/1 500 TABLET in 1 BOTTLE (64980-706-50)
64980-708-01 64980-708 HUMAN PRESCRIPTION DRUG Spironolactone Spironolactone TABLET ORAL 20250915 N/A ANDA ANDA219494 Rising Pharma Holdings, Inc. SPIRONOLACTONE 100 mg/1 100 TABLET in 1 BOTTLE (64980-708-01)
64980-708-50 64980-708 HUMAN PRESCRIPTION DRUG Spironolactone Spironolactone TABLET ORAL 20250915 N/A ANDA ANDA219494 Rising Pharma Holdings, Inc. SPIRONOLACTONE 100 mg/1 500 TABLET in 1 BOTTLE (64980-708-50)
64980-707-01 64980-707 HUMAN PRESCRIPTION DRUG Spironolactone Spironolactone TABLET ORAL 20250915 N/A ANDA ANDA219494 Rising Pharma Holdings, Inc. SPIRONOLACTONE 50 mg/1 100 TABLET in 1 BOTTLE (64980-707-01)
64980-707-50 64980-707 HUMAN PRESCRIPTION DRUG Spironolactone Spironolactone TABLET ORAL 20250915 N/A ANDA ANDA219494 Rising Pharma Holdings, Inc. SPIRONOLACTONE 50 mg/1 500 TABLET in 1 BOTTLE (64980-707-50)
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