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=ANDA215939"
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
70518-3921-0 70518-3921 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20231122 N/A ANDA ANDA215939 REMEDYREPACK INC. OXCARBAZEPINE 300 mg/1 100 POUCH in 1 BOX (70518-3921-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3921-1)
70518-3925-0 70518-3925 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20231126 N/A ANDA ANDA215939 REMEDYREPACK INC. OXCARBAZEPINE 600 mg/1 100 POUCH in 1 BOX (70518-3925-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3925-1)
70518-3940-0 70518-3940 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20231206 N/A ANDA ANDA215939 REMEDYREPACK INC. OXCARBAZEPINE 150 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3940-0)
70518-3940-1 70518-3940 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20240224 N/A ANDA ANDA215939 REMEDYREPACK INC. OXCARBAZEPINE 150 mg/1 100 POUCH in 1 BOX (70518-3940-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-3940-2)
55154-2138-0 55154-2138 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA215939 Cardinal Health 107, LLC OXCARBAZEPINE 300 mg/1 10 BLISTER PACK in 1 BAG (55154-2138-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
55154-2139-0 55154-2139 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA215939 Cardinal Health 107, LLC OXCARBAZEPINE 150 mg/1 10 BLISTER PACK in 1 BAG (55154-2139-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
60687-711-01 60687-711 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230131 N/A ANDA ANDA215939 American Health Packaging OXCARBAZEPINE 150 mg/1 100 BLISTER PACK in 1 CARTON (60687-711-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-711-11)
60687-722-01 60687-722 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA215939 American Health Packaging OXCARBAZEPINE 300 mg/1 100 BLISTER PACK in 1 CARTON (60687-722-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-722-11)
60687-733-01 60687-733 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230127 N/A ANDA ANDA215939 American Health Packaging OXCARBAZEPINE 600 mg/1 100 BLISTER PACK in 1 CARTON (60687-733-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-733-11)
0615-8447-39 0615-8447 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230113 N/A ANDA ANDA215939 NCS HealthCare of KY, LLC dba Vangard Labs OXCARBAZEPINE 150 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8447-39)
0615-8448-39 0615-8448 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230113 N/A ANDA ANDA215939 NCS HealthCare of KY, LLC dba Vangard Labs OXCARBAZEPINE 300 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8448-39)
31722-023-10 31722-023 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230310 N/A ANDA ANDA215939 Camber Pharmaceuticals, Inc. OXCARBAZEPINE 150 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (31722-023-10)
31722-023-31 31722-023 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20220111 N/A ANDA ANDA215939 Camber Pharmaceuticals, Inc. OXCARBAZEPINE 150 mg/1 10 BLISTER PACK in 1 CARTON (31722-023-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK
31722-024-01 31722-024 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20220111 N/A ANDA ANDA215939 Camber Pharmaceuticals, Inc. OXCARBAZEPINE 300 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (31722-024-01)
31722-024-05 31722-024 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230310 N/A ANDA ANDA215939 Camber Pharmaceuticals, Inc. OXCARBAZEPINE 300 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (31722-024-05)
31722-024-10 31722-024 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230310 N/A ANDA ANDA215939 Camber Pharmaceuticals, Inc. OXCARBAZEPINE 300 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (31722-024-10)
31722-024-31 31722-024 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20220111 N/A ANDA ANDA215939 Camber Pharmaceuticals, Inc. OXCARBAZEPINE 300 mg/1 10 BLISTER PACK in 1 CARTON (31722-024-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK
31722-025-01 31722-025 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20220111 N/A ANDA ANDA215939 Camber Pharmaceuticals, Inc. OXCARBAZEPINE 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (31722-025-01)
31722-025-05 31722-025 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230310 N/A ANDA ANDA215939 Camber Pharmaceuticals, Inc. OXCARBAZEPINE 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (31722-025-05)
31722-025-10 31722-025 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230310 N/A ANDA ANDA215939 Camber Pharmaceuticals, Inc. OXCARBAZEPINE 600 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (31722-025-10)
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