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=ANDA215995"
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
50090-7357-0 50090-7357 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20241017 N/A ANDA ANDA215995 A-S Medication Solutions BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 5 mg/1; 6.25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-7357-0)
50090-7357-2 50090-7357 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20241017 N/A ANDA ANDA215995 A-S Medication Solutions BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 5 mg/1; 6.25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-7357-2)
68462-878-01 68462-878 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20220126 N/A ANDA ANDA215995 GLENMARK PHARMACEUTICALS INC., USA BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 2.5 mg/1; 6.25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68462-878-01)
68462-878-05 68462-878 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20220126 N/A ANDA ANDA215995 GLENMARK PHARMACEUTICALS INC., USA BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 2.5 mg/1; 6.25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68462-878-05)
68462-878-30 68462-878 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20220126 N/A ANDA ANDA215995 GLENMARK PHARMACEUTICALS INC., USA BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 2.5 mg/1; 6.25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68462-878-30)
68462-880-01 68462-880 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20220126 N/A ANDA ANDA215995 GLENMARK PHARMACEUTICALS INC., USA BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 10 mg/1; 6.25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68462-880-01)
68462-880-05 68462-880 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20220126 N/A ANDA ANDA215995 GLENMARK PHARMACEUTICALS INC., USA BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 10 mg/1; 6.25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68462-880-05)
68462-880-30 68462-880 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20220126 N/A ANDA ANDA215995 GLENMARK PHARMACEUTICALS INC., USA BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 10 mg/1; 6.25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68462-880-30)
50090-6030-0 50090-6030 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20220706 N/A ANDA ANDA215995 A-S Medication Solutions BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 10 mg/1; 6.25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-6030-0)
68462-879-01 68462-879 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20220126 N/A ANDA ANDA215995 GLENMARK PHARMACEUTICALS INC., USA BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 5 mg/1; 6.25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68462-879-01)
68462-879-05 68462-879 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20220126 N/A ANDA ANDA215995 GLENMARK PHARMACEUTICALS INC., USA BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 5 mg/1; 6.25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68462-879-05)
68462-879-30 68462-879 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20220126 N/A ANDA ANDA215995 GLENMARK PHARMACEUTICALS INC., USA BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 5 mg/1; 6.25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68462-879-30)
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