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=ANDA077127"
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
62135-523-90 62135-523 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20230411 N/A ANDA ANDA077127 Chartwell RX, LLC NIFEDIPINE 90 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62135-523-90)
62135-521-90 62135-521 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20230411 N/A ANDA ANDA077127 Chartwell RX, LLC NIFEDIPINE 30 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62135-521-90)
62175-260-46 62175-260 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20051121 N/A ANDA ANDA077127 Lannett Company, Inc. NIFEDIPINE 30 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-260-46)
62175-261-46 62175-261 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20051121 N/A ANDA ANDA077127 Lannett Company, Inc. NIFEDIPINE 60 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-261-46)
62175-261-55 62175-261 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20051121 N/A ANDA ANDA077127 Lannett Company, Inc. NIFEDIPINE 60 mg/1 300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-261-55)
62175-262-32 62175-262 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20071003 N/A ANDA ANDA077127 Lannett Company, Inc. NIFEDIPINE 90 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-262-32)
62175-262-37 62175-262 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20071003 N/A ANDA ANDA077127 Lannett Company, Inc. NIFEDIPINE 90 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-262-37)
62175-262-46 62175-262 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20071003 N/A ANDA ANDA077127 Lannett Company, Inc. NIFEDIPINE 90 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-262-46)
62175-260-55 62175-260 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20051121 N/A ANDA ANDA077127 Lannett Company, Inc. NIFEDIPINE 30 mg/1 300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-260-55)
62175-261-37 62175-261 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20051121 N/A ANDA ANDA077127 Lannett Company, Inc. NIFEDIPINE 60 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-261-37)
62175-260-37 62175-260 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20051121 N/A ANDA ANDA077127 Lannett Company, Inc. NIFEDIPINE 30 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-260-37)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase