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=ANDA218015"
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
70010-188-03 70010-188 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20230929 N/A ANDA ANDA218015 Granules Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70010-188-03)
70010-188-10 70010-188 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20230929 N/A ANDA ANDA218015 Granules Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70010-188-10)
70010-189-03 70010-189 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20230929 N/A ANDA ANDA218015 Granules Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70010-189-03)
70010-189-10 70010-189 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20230929 N/A ANDA ANDA218015 Granules Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70010-189-10)
70010-187-03 70010-187 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20230929 N/A ANDA ANDA218015 Granules Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70010-187-03)
70010-187-10 70010-187 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20230929 N/A ANDA ANDA218015 Granules Pharmaceuticals Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70010-187-10)
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