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=ANDA090025"
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
50090-6378-0 50090-6378 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20230222 N/A ANDA ANDA090025 A-S Medication Solutions LEVETIRACETAM 1000 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-6378-0)
50090-6378-1 50090-6378 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20230222 N/A ANDA ANDA090025 A-S Medication Solutions LEVETIRACETAM 1000 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-6378-1)
50090-6378-2 50090-6378 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20230222 N/A ANDA ANDA090025 A-S Medication Solutions LEVETIRACETAM 1000 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (50090-6378-2)
68180-115-07 68180-115 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20090115 N/A ANDA ANDA090025 Lupin Pharmaceuticals, Inc. LEVETIRACETAM 1000 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68180-115-07)
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