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=ANDA203390"
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
46708-139-71 46708-139 HUMAN PRESCRIPTION DRUG Quetiapine Fumarate quetiapine fumarate TABLET, FILM COATED ORAL 20170221 N/A ANDA ANDA203390 Alembic Pharmaceuticals Limited QUETIAPINE FUMARATE 400 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (46708-139-71)
46708-135-31 46708-135 HUMAN PRESCRIPTION DRUG Quetiapine Fumarate quetiapine fumarate TABLET, FILM COATED ORAL 20170221 N/A ANDA ANDA203390 Alembic Pharmaceuticals Limited QUETIAPINE FUMARATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (46708-135-31)
46708-135-91 46708-135 HUMAN PRESCRIPTION DRUG Quetiapine Fumarate quetiapine fumarate TABLET, FILM COATED ORAL 20170221 N/A ANDA ANDA203390 Alembic Pharmaceuticals Limited QUETIAPINE FUMARATE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (46708-135-91)
46708-136-10 46708-136 HUMAN PRESCRIPTION DRUG Quetiapine Fumarate quetiapine fumarate TABLET, FILM COATED ORAL 20170221 N/A ANDA ANDA203390 Alembic Pharmaceuticals Limited QUETIAPINE FUMARATE 100 mg/1 100 TABLET, FILM COATED in 1 CARTON (46708-136-10)
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