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
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)
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)
62175-261-37 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)
62175-260-55 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)
62175-260-46 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)
63187-875-60 63187-875 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170703 N/A ANDA ANDA077127 Proficient Rx LP NIFEDIPINE 30 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-875-60)
63187-875-90 63187-875 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170703 N/A ANDA ANDA077127 Proficient Rx LP NIFEDIPINE 30 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-875-90)
63187-875-30 63187-875 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170703 N/A ANDA ANDA077127 Proficient Rx LP NIFEDIPINE 30 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-875-30)
68084-597-65 68084-597 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20230206 N/A ANDA ANDA077127 American Health Packaging NIFEDIPINE 30 mg/1 50 BLISTER PACK in 1 CARTON (68084-597-65) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-597-11)
68084-603-21 68084-603 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20120607 N/A ANDA ANDA077127 American Health Packaging NIFEDIPINE 90 mg/1 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-603-21) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-603-11)
68084-603-65 68084-603 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20230206 N/A ANDA ANDA077127 American Health Packaging NIFEDIPINE 90 mg/1 50 BLISTER PACK in 1 CARTON (68084-603-65) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-603-11)
68084-598-01 68084-598 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20120807 N/A ANDA ANDA077127 American Health Packaging NIFEDIPINE 60 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-598-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-598-11)
55154-8177-0 55154-8177 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20120807 N/A ANDA ANDA077127 Cardinal Health 107, LLC NIFEDIPINE 60 mg/1 10 BLISTER PACK in 1 BAG (55154-8177-0) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
68645-512-54 68645-512 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20051121 N/A ANDA ANDA077127 Legacy Pharmaceutical Packaging, LLC NIFEDIPINE 30 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68645-512-54)
68084-597-01 68084-597 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20120524 N/A ANDA ANDA077127 American Health Packaging NIFEDIPINE 30 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-597-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-597-11)
68084-598-65 68084-598 HUMAN PRESCRIPTION DRUG Nifedipine Nifedipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20230206 N/A ANDA ANDA077127 American Health Packaging NIFEDIPINE 60 mg/1 50 BLISTER PACK in 1 CARTON (68084-598-65) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-598-11)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase