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=ANDA078243"
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
68382-136-24 68382-136 HUMAN PRESCRIPTION DRUG Losartan Potassium Losartan Potassium TABLET, FILM COATED ORAL 20101004 N/A ANDA ANDA078243 Zydus Pharmaceuticals USA Inc. LOSARTAN POTASSIUM 50 mg/1 10000 TABLET, FILM COATED in 1 BOTTLE (68382-136-24)
68382-137-01 68382-137 HUMAN PRESCRIPTION DRUG Losartan Potassium Losartan Potassium TABLET, FILM COATED ORAL 20101004 N/A ANDA ANDA078243 Zydus Pharmaceuticals USA Inc. LOSARTAN POTASSIUM 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68382-137-01)
68382-137-06 68382-137 HUMAN PRESCRIPTION DRUG Losartan Potassium Losartan Potassium TABLET, FILM COATED ORAL 20101004 N/A ANDA ANDA078243 Zydus Pharmaceuticals USA Inc. LOSARTAN POTASSIUM 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68382-137-06)
68382-137-10 68382-137 HUMAN PRESCRIPTION DRUG Losartan Potassium Losartan Potassium TABLET, FILM COATED ORAL 20101004 N/A ANDA ANDA078243 Zydus Pharmaceuticals USA Inc. LOSARTAN POTASSIUM 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68382-137-10)
68382-137-16 68382-137 HUMAN PRESCRIPTION DRUG Losartan Potassium Losartan Potassium TABLET, FILM COATED ORAL 20101004 N/A ANDA ANDA078243 Zydus Pharmaceuticals USA Inc. LOSARTAN POTASSIUM 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68382-137-16)
68382-137-77 68382-137 HUMAN PRESCRIPTION DRUG Losartan Potassium Losartan Potassium TABLET, FILM COATED ORAL 20101004 N/A ANDA ANDA078243 Zydus Pharmaceuticals USA Inc. LOSARTAN POTASSIUM 100 mg/1 10 BLISTER PACK in 1 CARTON (68382-137-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-137-30)
68788-8639-1 68788-8639 HUMAN PRESCRIPTION DRUG Losortan Potassium Losartan Potassium TABLET, FILM COATED ORAL 20240418 N/A ANDA ANDA078243 Preferred Pharmaceuticals Inc. LOSARTAN POTASSIUM 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-8639-1)
68788-8639-3 68788-8639 HUMAN PRESCRIPTION DRUG Losortan Potassium Losartan Potassium TABLET, FILM COATED ORAL 20240418 N/A ANDA ANDA078243 Preferred Pharmaceuticals Inc. LOSARTAN POTASSIUM 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8639-3)
68788-8639-5 68788-8639 HUMAN PRESCRIPTION DRUG Losortan Potassium Losartan Potassium TABLET, FILM COATED ORAL 20240418 N/A ANDA ANDA078243 Preferred Pharmaceuticals Inc. LOSARTAN POTASSIUM 25 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (68788-8639-5)
68788-8639-6 68788-8639 HUMAN PRESCRIPTION DRUG Losortan Potassium Losartan Potassium TABLET, FILM COATED ORAL 20240418 N/A ANDA ANDA078243 Preferred Pharmaceuticals Inc. LOSARTAN POTASSIUM 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8639-6)
68788-8639-9 68788-8639 HUMAN PRESCRIPTION DRUG Losortan Potassium Losartan Potassium TABLET, FILM COATED ORAL 20240418 N/A ANDA ANDA078243 Preferred Pharmaceuticals Inc. LOSARTAN POTASSIUM 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8639-9)
72189-082-30 72189-082 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET, FILM COATED ORAL 20200616 N/A ANDA ANDA078243 DIRECT RX LOSARTAN POTASSIUM 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-082-30)
72189-082-90 72189-082 HUMAN PRESCRIPTION DRUG LOSARTAN POTASSIUM LOSARTAN POTASSIUM TABLET, FILM COATED ORAL 20200616 N/A ANDA ANDA078243 DIRECT RX LOSARTAN POTASSIUM 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72189-082-90)
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