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
31722-023-01 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)
31722-023-05 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)
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
0615-8567-39 0615-8567 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20250221 20260731 ANDA ANDA215939 NCS HealthCare of KY, LLC dba Vangard Labs OXCARBAZEPINE 600 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8567-39)
72603-271-01 72603-271 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20240901 N/A ANDA ANDA215939 NorthStar RxLLC OXCARBAZEPINE 300 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72603-271-01)
72603-271-02 72603-271 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20250428 N/A ANDA ANDA215939 NorthStar RxLLC OXCARBAZEPINE 300 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72603-271-02)
72865-285-01 72865-285 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20240718 N/A ANDA ANDA215939 XLCare Pharmaceuticals Inc. OXCARBAZEPINE 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72865-285-01)
72865-285-05 72865-285 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20240718 N/A ANDA ANDA215939 XLCare Pharmaceuticals Inc. OXCARBAZEPINE 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72865-285-05)
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)
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
60687-711-01 60687-711 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230202 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)
72865-283-01 72865-283 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20240718 N/A ANDA ANDA215939 XLCare Pharmaceuticals Inc. OXCARBAZEPINE 150 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72865-283-01)
72865-283-05 72865-283 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20240718 N/A ANDA ANDA215939 XLCare Pharmaceuticals Inc. OXCARBAZEPINE 150 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72865-283-05)
50268-680-15 50268-680 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230607 N/A ANDA ANDA215939 AvPAK OXCARBAZEPINE 300 mg/1 50 BLISTER PACK in 1 BOX (50268-680-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-680-11)
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
82804-209-72 82804-209 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20250318 N/A ANDA ANDA215939 Proficient Rx LP OXCARBAZEPINE 300 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (82804-209-72)
50268-681-15 50268-681 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230607 N/A ANDA ANDA215939 AvPAK OXCARBAZEPINE 600 mg/1 50 BLISTER PACK in 1 BOX (50268-681-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-681-11)
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