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=ANDA204316"
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
72865-269-05 72865-269 HUMAN PRESCRIPTION DRUG Quetiapine Fumarate Quetiapine Fumarate TABLET, FILM COATED ORAL 20240202 N/A ANDA ANDA204316 XLCare Pharmaceuticals Inc. QUETIAPINE FUMARATE 400 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72865-269-05)
72865-269-90 72865-269 HUMAN PRESCRIPTION DRUG Quetiapine Fumarate Quetiapine Fumarate TABLET, FILM COATED ORAL 20240722 N/A ANDA ANDA204316 XLCare Pharmaceuticals Inc. QUETIAPINE FUMARATE 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72865-269-90)
60760-764-30 60760-764 HUMAN PRESCRIPTION DRUG Quetiapine Fumarate Quetiapine Fumarate TABLET, FILM COATED ORAL 20250521 N/A ANDA ANDA204316 ST. MARY'S MEDICAL PARK PHARMACY QUETIAPINE FUMARATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-764-30)
72865-264-01 72865-264 HUMAN PRESCRIPTION DRUG Quetiapine Fumarate Quetiapine Fumarate TABLET, FILM COATED ORAL 20240202 N/A ANDA ANDA204316 XLCare Pharmaceuticals Inc. QUETIAPINE FUMARATE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72865-264-01)
72865-264-10 72865-264 HUMAN PRESCRIPTION DRUG Quetiapine Fumarate Quetiapine Fumarate TABLET, FILM COATED ORAL 20240202 N/A ANDA ANDA204316 XLCare Pharmaceuticals Inc. QUETIAPINE FUMARATE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (72865-264-10)
72865-264-90 72865-264 HUMAN PRESCRIPTION DRUG Quetiapine Fumarate Quetiapine Fumarate TABLET, FILM COATED ORAL 20240722 N/A ANDA ANDA204316 XLCare Pharmaceuticals Inc. QUETIAPINE FUMARATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72865-264-90)
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