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
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)
31722-023-10 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)
31722-023-05 31722-023 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230310 N/A ANDA ANDA215939 Camber Pharmaceuticals, Inc. OXCARBAZEPINE 150 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (31722-023-05)
71335-2548-1 71335-2548 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20250121 N/A ANDA ANDA215939 Bryant Ranch Prepack OXCARBAZEPINE 300 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2548-1)
71335-2548-2 71335-2548 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20250121 N/A ANDA ANDA215939 Bryant Ranch Prepack OXCARBAZEPINE 300 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-2548-2)
71335-2548-3 71335-2548 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20250121 N/A ANDA ANDA215939 Bryant Ranch Prepack OXCARBAZEPINE 300 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-2548-3)
71335-2548-4 71335-2548 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20250121 N/A ANDA ANDA215939 Bryant Ranch Prepack OXCARBAZEPINE 300 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71335-2548-4)
71335-2548-5 71335-2548 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20250121 N/A ANDA ANDA215939 Bryant Ranch Prepack OXCARBAZEPINE 300 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-2548-5)
31722-023-01 31722-023 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20220111 N/A ANDA ANDA215939 Camber Pharmaceuticals, Inc. OXCARBAZEPINE 150 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (31722-023-01)
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)
31722-025-31 31722-025 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20220111 N/A ANDA ANDA215939 Camber Pharmaceuticals, Inc. OXCARBAZEPINE 600 mg/1 10 BLISTER PACK in 1 CARTON (31722-025-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK
87063-208-60 87063-208 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20260519 N/A ANDA ANDA215939 ASCLEMED USA INC. OXCARBAZEPINE 300 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (87063-208-60)
87063-208-90 87063-208 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20260519 N/A ANDA ANDA215939 ASCLEMED USA INC. OXCARBAZEPINE 300 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (87063-208-90)
87063-208-01 87063-208 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20260519 N/A ANDA ANDA215939 ASCLEMED USA INC. OXCARBAZEPINE 300 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (87063-208-01)
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