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=ANDA203359"
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
33342-105-15 33342-105 HUMAN PRESCRIPTION DRUG Quetiapine fumarate Quetiapine fumarate TABLET, FILM COATED ORAL 20160614 N/A ANDA ANDA203359 Macleods Pharmaceuticals Limited QUETIAPINE FUMARATE 400 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (33342-105-15)
71335-1362-3 71335-1362 HUMAN PRESCRIPTION DRUG Quetiapine fumarate Quetiapine fumarate TABLET, FILM COATED ORAL 20240520 N/A ANDA ANDA203359 Bryant Ranch Prepack QUETIAPINE FUMARATE 200 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-1362-3)
71335-1362-2 71335-1362 HUMAN PRESCRIPTION DRUG Quetiapine fumarate Quetiapine fumarate TABLET, FILM COATED ORAL 20240520 N/A ANDA ANDA203359 Bryant Ranch Prepack QUETIAPINE FUMARATE 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-1362-2)
71335-1362-1 71335-1362 HUMAN PRESCRIPTION DRUG Quetiapine fumarate Quetiapine fumarate TABLET, FILM COATED ORAL 20191003 N/A ANDA ANDA203359 Bryant Ranch Prepack QUETIAPINE FUMARATE 200 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1362-1)
33342-105-39 33342-105 HUMAN PRESCRIPTION DRUG Quetiapine fumarate Quetiapine fumarate TABLET, FILM COATED ORAL 20160614 N/A ANDA ANDA203359 Macleods Pharmaceuticals Limited QUETIAPINE FUMARATE 400 mg/1 9 BLISTER PACK in 1 CARTON (33342-105-39) / 10 TABLET, FILM COATED in 1 BLISTER PACK
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