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=ANDA209922"
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
43547-550-10 43547-550 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE potassium chloride extended-release TABLET ORAL 20190430 N/A ANDA ANDA209922 Solco Healthcare LLC POTASSIUM CHLORIDE 1500 mg/1 100 TABLET in 1 BOTTLE (43547-550-10)
43547-550-11 43547-550 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE potassium chloride extended-release TABLET ORAL 20190430 N/A ANDA ANDA209922 Solco Healthcare LLC POTASSIUM CHLORIDE 1500 mg/1 1000 TABLET in 1 BOTTLE (43547-550-11)
43547-550-50 43547-550 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE potassium chloride extended-release TABLET ORAL 20190430 N/A ANDA ANDA209922 Solco Healthcare LLC POTASSIUM CHLORIDE 1500 mg/1 500 TABLET in 1 BOTTLE (43547-550-50)
43547-551-10 43547-551 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE potassium chloride extended-release TABLET ORAL 20190430 N/A ANDA ANDA209922 Solco Healthcare LLC POTASSIUM CHLORIDE 1125 mg/1 100 TABLET in 1 BOTTLE (43547-551-10)
43547-549-50 43547-549 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE potassium chloride extended-release TABLET ORAL 20190430 N/A ANDA ANDA209922 Solco Healthcare LLC POTASSIUM CHLORIDE 750 mg/1 500 TABLET in 1 BOTTLE (43547-549-50)
43547-549-10 43547-549 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE potassium chloride extended-release TABLET ORAL 20190430 N/A ANDA ANDA209922 Solco Healthcare LLC POTASSIUM CHLORIDE 750 mg/1 100 TABLET in 1 BOTTLE (43547-549-10)
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