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=ANDA216598"
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
60219-2039-1 60219-2039 HUMAN PRESCRIPTION DRUG prochlorperazine maleate prochlorperazine maleate TABLET, FILM COATED ORAL 20230421 N/A ANDA ANDA216598 Amneal Pharmaceuticals NY LLC PROCHLORPERAZINE MALEATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60219-2039-1)
60219-2039-7 60219-2039 HUMAN PRESCRIPTION DRUG prochlorperazine maleate prochlorperazine maleate TABLET, FILM COATED ORAL 20230421 N/A ANDA ANDA216598 Amneal Pharmaceuticals NY LLC PROCHLORPERAZINE MALEATE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60219-2039-7)
60219-2038-1 60219-2038 HUMAN PRESCRIPTION DRUG prochlorperazine maleate prochlorperazine maleate TABLET, FILM COATED ORAL 20230421 N/A ANDA ANDA216598 Amneal Pharmaceuticals NY LLC PROCHLORPERAZINE MALEATE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60219-2038-1)
60219-2038-7 60219-2038 HUMAN PRESCRIPTION DRUG prochlorperazine maleate prochlorperazine maleate TABLET, FILM COATED ORAL 20230421 N/A ANDA ANDA216598 Amneal Pharmaceuticals NY LLC PROCHLORPERAZINE MALEATE 5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60219-2038-7)
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