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=ANDA203012"
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
46708-133-10 46708-133 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA203012 Alembic Pharmaceuticals Limited OLMESARTAN MEDOXOMIL 40 mg/1 100 TABLET, FILM COATED in 1 CARTON (46708-133-10)
46708-133-30 46708-133 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA203012 Alembic Pharmaceuticals Limited OLMESARTAN MEDOXOMIL 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (46708-133-30)
46708-133-90 46708-133 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA203012 Alembic Pharmaceuticals Limited OLMESARTAN MEDOXOMIL 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (46708-133-90)
46708-133-91 46708-133 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA203012 Alembic Pharmaceuticals Limited OLMESARTAN MEDOXOMIL 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (46708-133-91)
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