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=ANDA077666"
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
60505-0248-8 60505-0248 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20070822 N/A ANDA ANDA077666 Apotex Corp. MIRTAZAPINE 30 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (60505-0248-8)
60505-0249-1 60505-0249 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20070822 N/A ANDA ANDA077666 Apotex Corp. MIRTAZAPINE 45 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (60505-0249-1)
60505-0249-3 60505-0249 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20070822 N/A ANDA ANDA077666 Apotex Corp. MIRTAZAPINE 45 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (60505-0249-3)
60505-0249-5 60505-0249 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20070822 N/A ANDA ANDA077666 Apotex Corp. MIRTAZAPINE 45 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (60505-0249-5)
60505-0249-8 60505-0249 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20070822 N/A ANDA ANDA077666 Apotex Corp. MIRTAZAPINE 45 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (60505-0249-8)
60505-0247-3 60505-0247 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20070822 N/A ANDA ANDA077666 Apotex Corp. MIRTAZAPINE 15 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (60505-0247-3)
67046-1590-3 67046-1590 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20250916 N/A ANDA ANDA077666 Coupler LLC MIRTAZAPINE 15 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1590-3)
60505-0247-5 60505-0247 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20070822 N/A ANDA ANDA077666 Apotex Corp. MIRTAZAPINE 15 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (60505-0247-5)
60505-0247-8 60505-0247 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20070822 N/A ANDA ANDA077666 Apotex Corp. MIRTAZAPINE 15 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (60505-0247-8)
55154-7297-0 55154-7297 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20070822 N/A ANDA ANDA077666 Cardinal Health 107, LLC MIRTAZAPINE 15 mg/1 10 BLISTER PACK in 1 BAG (55154-7297-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
43353-378-60 43353-378 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20240628 N/A ANDA ANDA077666 Aphena Pharma Solutions - Tennessee, LLC MIRTAZAPINE 30 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (43353-378-60)
43353-378-15 43353-378 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20180810 N/A ANDA ANDA077666 Aphena Pharma Solutions - Tennessee, LLC MIRTAZAPINE 30 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (43353-378-15)
43353-378-30 43353-378 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20180810 N/A ANDA ANDA077666 Aphena Pharma Solutions - Tennessee, LLC MIRTAZAPINE 30 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (43353-378-30)
43353-378-45 43353-378 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20180810 N/A ANDA ANDA077666 Aphena Pharma Solutions - Tennessee, LLC MIRTAZAPINE 30 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (43353-378-45)
0904-6519-61 0904-6519 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20070822 N/A ANDA ANDA077666 Major Pharmaceuticals MIRTAZAPINE 15 mg/1 100 BLISTER PACK in 1 CARTON (0904-6519-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
63739-098-10 63739-098 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20191115 20270331 ANDA ANDA077666 McKesson Corporation dba SKY Packaging MIRTAZAPINE 15 mg/1 10 BLISTER PACK in 1 BOX (63739-098-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
63739-099-10 63739-099 HUMAN PRESCRIPTION DRUG Mirtazapine Mirtazapine TABLET, FILM COATED ORAL 20191115 20270331 ANDA ANDA077666 McKesson Corporation dba SKY Packaging MIRTAZAPINE 30 mg/1 10 BLISTER PACK in 1 BOX (63739-099-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase