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=ANDA217922"
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
59651-678-01 59651-678 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20260121 N/A ANDA ANDA217922 Aurobindo Pharma Limited BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 2.5 mg/1; 6.25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (59651-678-01)
59651-678-05 59651-678 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20260121 N/A ANDA ANDA217922 Aurobindo Pharma Limited BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 2.5 mg/1; 6.25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (59651-678-05)
59651-678-30 59651-678 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20260121 N/A ANDA ANDA217922 Aurobindo Pharma Limited BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 2.5 mg/1; 6.25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (59651-678-30)
59651-679-01 59651-679 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20260121 N/A ANDA ANDA217922 Aurobindo Pharma Limited BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 5 mg/1; 6.25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (59651-679-01)
59651-679-05 59651-679 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20260121 N/A ANDA ANDA217922 Aurobindo Pharma Limited BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 5 mg/1; 6.25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (59651-679-05)
59651-679-30 59651-679 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20260121 N/A ANDA ANDA217922 Aurobindo Pharma Limited BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 5 mg/1; 6.25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (59651-679-30)
59651-680-01 59651-680 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20260121 N/A ANDA ANDA217922 Aurobindo Pharma Limited BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 10 mg/1; 6.25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (59651-680-01)
59651-680-05 59651-680 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20260121 N/A ANDA ANDA217922 Aurobindo Pharma Limited BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 10 mg/1; 6.25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (59651-680-05)
59651-680-30 59651-680 HUMAN PRESCRIPTION DRUG Bisoprolol Fumarate and Hydrochlorothiazide Bisoprolol Fumarate and Hydrochlorothiazide TABLET, FILM COATED ORAL 20260121 N/A ANDA ANDA217922 Aurobindo Pharma Limited BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE 10 mg/1; 6.25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (59651-680-30)
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