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=ANDA076921"
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
68788-7324-6 68788-7324 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20201123 N/A ANDA ANDA076921 Preferred Pharmaceuticals Inc. MIRTAZAPINE 30 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-7324-6)
68788-7324-9 68788-7324 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20201123 N/A ANDA ANDA076921 Preferred Pharmaceuticals Inc. MIRTAZAPINE 30 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-7324-9)
71335-2412-1 71335-2412 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20240610 N/A ANDA ANDA076921 Bryant Ranch Prepack MIRTAZAPINE 7.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2412-1)
68788-7492-1 68788-7492 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20200601 N/A ANDA ANDA076921 Preferred Pharmaceuticals, Inc. MIRTAZAPINE 15 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68788-7492-1)
68788-7492-3 68788-7492 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20200601 N/A ANDA ANDA076921 Preferred Pharmaceuticals, Inc. MIRTAZAPINE 15 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-7492-3)
68788-7492-6 68788-7492 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20200601 N/A ANDA ANDA076921 Preferred Pharmaceuticals, Inc. MIRTAZAPINE 15 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-7492-6)
68788-7492-9 68788-7492 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20200601 N/A ANDA ANDA076921 Preferred Pharmaceuticals, Inc. MIRTAZAPINE 15 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-7492-9)
68788-7754-3 68788-7754 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20200701 N/A ANDA ANDA076921 Preferred Pharmaceuticals, Inc. MIRTAZAPINE 45 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-7754-3)
68788-7754-6 68788-7754 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20200701 N/A ANDA ANDA076921 Preferred Pharmaceuticals, Inc. MIRTAZAPINE 45 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-7754-6)
68788-7754-9 68788-7754 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20200701 N/A ANDA ANDA076921 Preferred Pharmaceuticals, Inc. MIRTAZAPINE 45 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-7754-9)
70518-1309-0 70518-1309 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20180718 N/A ANDA ANDA076921 REMEDYREPACK INC. MIRTAZAPINE 30 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1309-0)
70518-1309-2 70518-1309 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20220111 N/A ANDA ANDA076921 REMEDYREPACK INC. MIRTAZAPINE 30 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1309-2)
49999-629-60 49999-629 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20090817 20250930 ANDA ANDA076921 Quality Care Products LLC MIRTAZAPINE 15 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (49999-629-60)
13107-001-01 13107-001 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20090817 N/A ANDA ANDA076921 Aurolife Pharma LLC MIRTAZAPINE 7.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (13107-001-01)
13107-001-05 13107-001 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20090817 N/A ANDA ANDA076921 Aurolife Pharma LLC MIRTAZAPINE 7.5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (13107-001-05)
13107-001-30 13107-001 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20090817 N/A ANDA ANDA076921 Aurolife Pharma LLC MIRTAZAPINE 7.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (13107-001-30)
13107-001-60 13107-001 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20090817 N/A ANDA ANDA076921 Aurolife Pharma LLC MIRTAZAPINE 7.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (13107-001-60)
13107-001-90 13107-001 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20090817 N/A ANDA ANDA076921 Aurolife Pharma LLC MIRTAZAPINE 7.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (13107-001-90)
13107-003-01 13107-003 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20090817 N/A ANDA ANDA076921 Aurolife Pharma LLC MIRTAZAPINE 30 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (13107-003-01)
13107-003-05 13107-003 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20090817 N/A ANDA ANDA076921 Aurolife Pharma LLC MIRTAZAPINE 30 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (13107-003-05)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase