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=ANDA209635"
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
50228-382-60 50228-382 HUMAN PRESCRIPTION DRUG Quetiapine Extended Release Quetiapine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20171129 N/A ANDA ANDA209635 ScieGen Pharmaceuticals, Inc QUETIAPINE FUMARATE 200 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-382-60)
71093-135-02 71093-135 HUMAN PRESCRIPTION DRUG Quetiapine Extended Release Quetiapine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190130 N/A ANDA ANDA209635 ACI Healthcare USA, Inc. QUETIAPINE FUMARATE 50 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71093-135-02)
71093-136-02 71093-136 HUMAN PRESCRIPTION DRUG Quetiapine Extended Release Quetiapine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180201 N/A ANDA ANDA209635 ACI Healthcare USA, Inc. QUETIAPINE FUMARATE 150 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71093-136-02)
72189-519-30 72189-519 HUMAN PRESCRIPTION DRUG Quetiapine Fumarate ER Quetiapine Fumarate ER TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231101 N/A ANDA ANDA209635 Direct_Rx QUETIAPINE FUMARATE 200 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-519-30)
71093-139-02 71093-139 HUMAN PRESCRIPTION DRUG Quetiapine Extended Release Quetiapine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180201 N/A ANDA ANDA209635 ACI Healthcare USA, Inc. QUETIAPINE FUMARATE 400 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71093-139-02)
70518-4051-0 70518-4051 HUMAN PRESCRIPTION DRUG Quetiapine Extended Release Quetiapine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240413 N/A ANDA ANDA209635 REMEDYREPACK INC. QUETIAPINE FUMARATE 150 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4051-0)
60760-866-30 60760-866 HUMAN PRESCRIPTION DRUG Quetiapine Extended Release Quetiapine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250519 N/A ANDA ANDA209635 ST. MARY'S MEDICAL PARK PHARMACY QUETIAPINE FUMARATE 200 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-866-30)
71093-137-02 71093-137 HUMAN PRESCRIPTION DRUG Quetiapine Extended Release Quetiapine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180201 N/A ANDA ANDA209635 ACI Healthcare USA, Inc. QUETIAPINE FUMARATE 200 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71093-137-02)
71093-138-02 71093-138 HUMAN PRESCRIPTION DRUG Quetiapine Extended Release Quetiapine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180201 N/A ANDA ANDA209635 ACI Healthcare USA, Inc. QUETIAPINE FUMARATE 300 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71093-138-02)
72189-586-30 72189-586 HUMAN PRESCRIPTION DRUG Quetiapine Fumarate ER Quetiapine Fumarate ER TABLET, FILM COATED, EXTENDED RELEASE ORAL 20241002 N/A ANDA ANDA209635 Direct_rx QUETIAPINE FUMARATE 150 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-586-30)
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