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=ANDA078042"
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
71093-123-12 71093-123 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20230930 N/A ANDA ANDA078042 ACI Healthcare USA, Inc. LEVETIRACETAM 250 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71093-123-12)
71093-124-05 71093-124 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20230930 N/A ANDA ANDA078042 ACI Healthcare USA, Inc. LEVETIRACETAM 500 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (71093-124-05)
71093-124-12 71093-124 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20230930 N/A ANDA ANDA078042 ACI Healthcare USA, Inc. LEVETIRACETAM 500 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71093-124-12)
71093-125-12 71093-125 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20230930 N/A ANDA ANDA078042 ACI Healthcare USA, Inc. LEVETIRACETAM 750 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71093-125-12)
71093-126-02 71093-126 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20230930 N/A ANDA ANDA078042 ACI Healthcare USA, Inc. LEVETIRACETAM 1000 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71093-126-02)
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