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=ANDA090428"
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
46708-447-91 46708-447 HUMAN PRESCRIPTION DRUG Losartan Potassium Losartan Potassium TABLET, FILM COATED ORAL 20160523 N/A ANDA ANDA090428 Alembic Pharmaceuticals Limited LOSARTAN POTASSIUM 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (46708-447-91)
46708-445-31 46708-445 HUMAN PRESCRIPTION DRUG Losartan Potassium Losartan Potassium TABLET, FILM COATED ORAL 20160523 N/A ANDA ANDA090428 Alembic Pharmaceuticals Limited LOSARTAN POTASSIUM 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (46708-445-31)
46708-445-90 46708-445 HUMAN PRESCRIPTION DRUG Losartan Potassium Losartan Potassium TABLET, FILM COATED ORAL 20160523 N/A ANDA ANDA090428 Alembic Pharmaceuticals Limited LOSARTAN POTASSIUM 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (46708-445-90)
46708-445-91 46708-445 HUMAN PRESCRIPTION DRUG Losartan Potassium Losartan Potassium TABLET, FILM COATED ORAL 20160523 N/A ANDA ANDA090428 Alembic Pharmaceuticals Limited LOSARTAN POTASSIUM 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (46708-445-91)
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