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=ANDA219869"
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
31722-755-10 31722-755 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260527 N/A ANDA ANDA219869 Camber Pharmaceuticals, Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (31722-755-10)
31722-755-30 31722-755 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260527 N/A ANDA ANDA219869 Camber Pharmaceuticals, Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-755-30)
31722-755-90 31722-755 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260527 N/A ANDA ANDA219869 Camber Pharmaceuticals, Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (31722-755-90)
31722-757-10 31722-757 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260527 N/A ANDA ANDA219869 Camber Pharmaceuticals, Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (31722-757-10)
31722-757-30 31722-757 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260527 N/A ANDA ANDA219869 Camber Pharmaceuticals, Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-757-30)
31722-757-90 31722-757 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260527 N/A ANDA ANDA219869 Camber Pharmaceuticals, Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25 mg/1; 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (31722-757-90)
31722-756-10 31722-756 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260527 N/A ANDA ANDA219869 Camber Pharmaceuticals, Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (31722-756-10)
31722-756-30 31722-756 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260527 N/A ANDA ANDA219869 Camber Pharmaceuticals, Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-756-30)
31722-756-90 31722-756 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED ORAL 20260527 N/A ANDA ANDA219869 Camber Pharmaceuticals, Inc. HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5 mg/1; 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (31722-756-90)
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