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
60760-315-90 60760-315 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20190530 N/A ANDA ANDA040907 St. Mary's Medical Park Pharmacy HYDROCHLOROTHIAZIDE 25 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (60760-315-90)
68788-8517-3 68788-8517 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20230901 N/A ANDA ANDA040907 Preferred Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE 25 mg/1 30 TABLET in 1 BOTTLE (68788-8517-3)
68788-8517-6 68788-8517 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20230901 N/A ANDA ANDA040907 Preferred Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE 25 mg/1 60 TABLET in 1 BOTTLE (68788-8517-6)
68788-8517-9 68788-8517 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20230901 N/A ANDA ANDA040907 Preferred Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE 25 mg/1 90 TABLET in 1 BOTTLE (68788-8517-9)
50090-0141-0 50090-0141 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20141128 N/A ANDA ANDA040907 A-S Medication Solutions HYDROCHLOROTHIAZIDE 25 mg/1 90 TABLET in 1 BOTTLE (50090-0141-0)
67296-2043-3 67296-2043 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20090702 N/A ANDA ANDA040907 Redpharm drug HYDROCHLOROTHIAZIDE 25 mg/1 30 TABLET in 1 BOTTLE (67296-2043-3)
67046-1016-3 67046-1016 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20241111 N/A ANDA ANDA040907 Coupler LLC HYDROCHLOROTHIAZIDE 25 mg/1 30 TABLET in 1 BLISTER PACK (67046-1016-3)
72789-303-01 72789-303 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20220302 N/A ANDA ANDA040907 PD-Rx Pharmaceuticals, Inc. HYDROCHLOROTHIAZIDE 50 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (72789-303-01)
71205-419-14 71205-419 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20240328 N/A ANDA ANDA040907 Proficient Rx LP HYDROCHLOROTHIAZIDE 25 mg/1 14 TABLET in 1 BOTTLE (71205-419-14)
71205-419-30 71205-419 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20200301 N/A ANDA ANDA040907 Proficient Rx LP HYDROCHLOROTHIAZIDE 25 mg/1 30 TABLET in 1 BOTTLE (71205-419-30)
71205-419-60 71205-419 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20200301 N/A ANDA ANDA040907 Proficient Rx LP HYDROCHLOROTHIAZIDE 25 mg/1 60 TABLET in 1 BOTTLE (71205-419-60)
71205-419-90 71205-419 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20200301 N/A ANDA ANDA040907 Proficient Rx LP HYDROCHLOROTHIAZIDE 25 mg/1 90 TABLET in 1 BOTTLE (71205-419-90)
68788-8417-3 68788-8417 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20230410 N/A ANDA ANDA040907 Preferred Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE 50 mg/1 30 TABLET in 1 BOTTLE (68788-8417-3)
68788-8417-6 68788-8417 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20230410 N/A ANDA ANDA040907 Preferred Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE 50 mg/1 60 TABLET in 1 BOTTLE (68788-8417-6)
68788-8417-9 68788-8417 HUMAN PRESCRIPTION DRUG Hydrochlorothiazide Hydrochlorothiazide TABLET ORAL 20230410 N/A ANDA ANDA040907 Preferred Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE 50 mg/1 90 TABLET in 1 BOTTLE (68788-8417-9)
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)
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