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=ANDA203562"
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
71335-1109-4 71335-1109 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20211220 N/A ANDA ANDA203562 Bryant Ranch Prepack POTASSIUM CHLORIDE 1500 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1109-4)
71335-1109-5 71335-1109 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20211220 N/A ANDA ANDA203562 Bryant Ranch Prepack POTASSIUM CHLORIDE 1500 mg/1 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1109-5)
71335-1109-6 71335-1109 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20211220 N/A ANDA ANDA203562 Bryant Ranch Prepack POTASSIUM CHLORIDE 1500 mg/1 7 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1109-6)
71335-1109-7 71335-1109 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20211220 N/A ANDA ANDA203562 Bryant Ranch Prepack POTASSIUM CHLORIDE 1500 mg/1 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1109-7)
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