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
70518-3940-1 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)
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)
50268-679-15 50268-679 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20230607 N/A ANDA ANDA215939 AvPAK OXCARBAZEPINE 150 mg/1 50 BLISTER PACK in 1 BOX (50268-679-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-679-11)
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)
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)
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
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
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)
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