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=ANDA088072"
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
42806-513-30 42806-513 HUMAN PRESCRIPTION DRUG QUINIDINE SULFATE quinidine sulfate tablet TABLET ORAL 20220102 N/A ANDA ANDA088072 EPIC PHARMA, LLC QUINIDINE SULFATE 200 mg/1 30 TABLET in 1 BOTTLE (42806-513-30)
42806-513-01 42806-513 HUMAN PRESCRIPTION DRUG QUINIDINE SULFATE quinidine sulfate tablet TABLET ORAL 20211215 N/A ANDA ANDA088072 EPIC PHARMA, LLC QUINIDINE SULFATE 200 mg/1 100 TABLET in 1 BOTTLE (42806-513-01)
42806-512-30 42806-512 HUMAN PRESCRIPTION DRUG QUINIDINE SULFATE quinidine sulfate tablet TABLET ORAL 20220102 N/A ANDA ANDA088072 EPIC PHARMA, LLC QUINIDINE SULFATE 300 mg/1 30 TABLET in 1 BOTTLE (42806-512-30)
42806-512-01 42806-512 HUMAN PRESCRIPTION DRUG QUINIDINE SULFATE quinidine sulfate tablet TABLET ORAL 20211215 N/A ANDA ANDA088072 EPIC PHARMA, LLC QUINIDINE SULFATE 300 mg/1 100 TABLET in 1 BOTTLE (42806-512-01)
0185-1047-01 0185-1047 HUMAN PRESCRIPTION DRUG Quinidine Sulfate Quinidine Sulfate TABLET ORAL 19830926 20250531 ANDA ANDA088072 Eon Labs, Inc. QUINIDINE SULFATE 300 mg/1 100 TABLET in 1 BOTTLE (0185-1047-01)
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