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=ANDA211049"
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
0527-2425-32 0527-2425 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL Olmesartan medoxomil TABLET, FILM COATED ORAL 20190305 N/A ANDA ANDA211049 Lannett Company, Inc. OLMESARTAN MEDOXOMIL 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-2425-32)
0527-2425-46 0527-2425 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL Olmesartan medoxomil TABLET, FILM COATED ORAL 20190305 N/A ANDA ANDA211049 Lannett Company, Inc. OLMESARTAN MEDOXOMIL 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-2425-46)
0527-2426-32 0527-2426 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL Olmesartan medoxomil TABLET, FILM COATED ORAL 20190305 N/A ANDA ANDA211049 Lannett Company, Inc. OLMESARTAN MEDOXOMIL 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-2426-32)
0527-2426-46 0527-2426 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL Olmesartan medoxomil TABLET, FILM COATED ORAL 20190305 N/A ANDA ANDA211049 Lannett Company, Inc. OLMESARTAN MEDOXOMIL 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-2426-46)
0527-2427-32 0527-2427 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL Olmesartan medoxomil TABLET, FILM COATED ORAL 20190305 N/A ANDA ANDA211049 Lannett Company, Inc. OLMESARTAN MEDOXOMIL 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-2427-32)
0527-2427-46 0527-2427 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL Olmesartan medoxomil TABLET, FILM COATED ORAL 20190305 N/A ANDA ANDA211049 Lannett Company, Inc. OLMESARTAN MEDOXOMIL 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-2427-46)
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