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=ANDA040907"
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
50090-0140-0 50090-0140 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20141128 N/A ANDA ANDA040907 A-S Medication Solutions HYDROCHLOROTHIAZIDE 25 mg/1 30 TABLET in 1 BOTTLE (50090-0140-0)
50090-0140-1 50090-0140 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20141128 N/A ANDA ANDA040907 A-S Medication Solutions HYDROCHLOROTHIAZIDE 25 mg/1 100 TABLET in 1 BOTTLE (50090-0140-1)
50090-0140-8 50090-0140 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20141128 N/A ANDA ANDA040907 A-S Medication Solutions HYDROCHLOROTHIAZIDE 25 mg/1 200 TABLET in 1 BOTTLE (50090-0140-8)
76282-154-01 76282-154 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20160830 N/A ANDA ANDA040907 Exelan Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE 25 mg/1 100 TABLET in 1 BOTTLE (76282-154-01)
76282-154-05 76282-154 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20160830 N/A ANDA ANDA040907 Exelan Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE 25 mg/1 500 TABLET in 1 BOTTLE (76282-154-05)
76282-154-10 76282-154 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20160830 N/A ANDA ANDA040907 Exelan Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE 25 mg/1 1000 TABLET in 1 BOTTLE (76282-154-10)
76282-154-90 76282-154 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20160830 N/A ANDA ANDA040907 Exelan Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE 25 mg/1 90 TABLET in 1 BOTTLE (76282-154-90)
29300-129-01 29300-129 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20090702 N/A ANDA ANDA040907 Unichem Pharmaceuticals (USA), Inc. HYDROCHLOROTHIAZIDE 50 mg/1 100 TABLET in 1 BOTTLE (29300-129-01)
29300-129-05 29300-129 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20090702 N/A ANDA ANDA040907 Unichem Pharmaceuticals (USA), Inc. HYDROCHLOROTHIAZIDE 50 mg/1 500 TABLET in 1 BOTTLE (29300-129-05)
29300-129-10 29300-129 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20090702 N/A ANDA ANDA040907 Unichem Pharmaceuticals (USA), Inc. HYDROCHLOROTHIAZIDE 50 mg/1 1000 TABLET in 1 BOTTLE (29300-129-10)
82804-031-30 82804-031 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20231024 N/A ANDA ANDA040907 Proficient Rx LP HYDROCHLOROTHIAZIDE 50 mg/1 30 TABLET in 1 BOTTLE (82804-031-30)
82804-031-60 82804-031 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20231024 N/A ANDA ANDA040907 Proficient Rx LP HYDROCHLOROTHIAZIDE 50 mg/1 60 TABLET in 1 BOTTLE (82804-031-60)
82804-031-90 82804-031 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20231024 N/A ANDA ANDA040907 Proficient Rx LP HYDROCHLOROTHIAZIDE 50 mg/1 90 TABLET in 1 BOTTLE (82804-031-90)
29300-128-01 29300-128 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20090702 N/A ANDA ANDA040907 Unichem Pharmaceuticals (USA), Inc. HYDROCHLOROTHIAZIDE 25 mg/1 100 TABLET in 1 BOTTLE (29300-128-01)
29300-128-05 29300-128 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20090702 N/A ANDA ANDA040907 Unichem Pharmaceuticals (USA), Inc. HYDROCHLOROTHIAZIDE 25 mg/1 500 TABLET in 1 BOTTLE (29300-128-05)
29300-128-10 29300-128 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20090702 N/A ANDA ANDA040907 Unichem Pharmaceuticals (USA), Inc. HYDROCHLOROTHIAZIDE 25 mg/1 1000 TABLET in 1 BOTTLE (29300-128-10)
29300-128-50 29300-128 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20090702 N/A ANDA ANDA040907 Unichem Pharmaceuticals (USA), Inc. HYDROCHLOROTHIAZIDE 25 mg/1 5000 TABLET in 1 BOTTLE (29300-128-50)
51655-422-26 51655-422 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20221229 N/A ANDA ANDA040907 Northwind Health Company, LLC HYDROCHLOROTHIAZIDE 50 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (51655-422-26)
51655-422-52 51655-422 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20230606 N/A ANDA ANDA040907 Northwind Health Company, LLC HYDROCHLOROTHIAZIDE 50 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-422-52)
55700-006-30 55700-006 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20090702 20260731 ANDA ANDA040907 Lake Erie Medical DBA Quality Care Products LLC HYDROCHLOROTHIAZIDE 25 mg/1 30 TABLET in 1 BOTTLE (55700-006-30)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase