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=ANDA216321"
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
72888-098-00 72888-098 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20230630 N/A ANDA ANDA216321 Advagen Pharma Ltd. POTASSIUM CHLORIDE 1125 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-098-00)
72888-098-01 72888-098 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20230630 N/A ANDA ANDA216321 Advagen Pharma Ltd. POTASSIUM CHLORIDE 1125 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-098-01)
72888-099-00 72888-099 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20230630 N/A ANDA ANDA216321 Advagen Pharma Ltd. POTASSIUM CHLORIDE 1500 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-099-00)
72888-099-01 72888-099 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20230630 N/A ANDA ANDA216321 Advagen Pharma Ltd. POTASSIUM CHLORIDE 1500 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-099-01)
72888-097-01 72888-097 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20230630 N/A ANDA ANDA216321 Advagen Pharma Ltd. POTASSIUM CHLORIDE 750 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-097-01)
72888-097-00 72888-097 HUMAN PRESCRIPTION DRUG POTASSIUM CHLORIDE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE ORAL 20230630 N/A ANDA ANDA216321 Advagen Pharma Ltd. POTASSIUM CHLORIDE 750 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-097-00)
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