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=NDA021985"
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
66993-141-30 66993-141 HUMAN PRESCRIPTION DRUG Aliskiren aliskiren hemifumarate TABLET, FILM COATED ORAL 20190304 N/A NDA AUTHORIZED GENERIC NDA021985 Prasco Laboratories ALISKIREN HEMIFUMARATE 150 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (66993-141-30)
66993-142-30 66993-142 HUMAN PRESCRIPTION DRUG Aliskiren aliskiren hemifumarate TABLET, FILM COATED ORAL 20190304 N/A NDA AUTHORIZED GENERIC NDA021985 Prasco Laboratories ALISKIREN HEMIFUMARATE 300 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (66993-142-30)
70839-150-30 70839-150 HUMAN PRESCRIPTION DRUG Tekturna aliskiren hemifumarate TABLET, FILM COATED ORAL 20170101 N/A NDA NDA021985 LXO US Inc. ALISKIREN HEMIFUMARATE 150 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70839-150-30)
50090-2985-0 50090-2985 HUMAN PRESCRIPTION DRUG TEKTURNA aliskiren hemifumarate TABLET, FILM COATED ORAL 20170425 N/A NDA NDA021985 A-S Medication Solutions ALISKIREN HEMIFUMARATE 300 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-2985-0)
70839-300-30 70839-300 HUMAN PRESCRIPTION DRUG Tekturna aliskiren hemifumarate TABLET, FILM COATED ORAL 20170101 N/A NDA NDA021985 LXO US Inc. ALISKIREN HEMIFUMARATE 300 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70839-300-30)
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