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=ANDA078069"
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
68084-867-01 68084-867 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20141203 20240630 ANDA ANDA078069 American Health Packaging OXCARBAZEPINE 600 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-867-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-867-11)
71335-0090-3 71335-0090 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20200423 N/A ANDA ANDA078069 Bryant Ranch Prepack OXCARBAZEPINE 300 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0090-3)
71335-0090-5 71335-0090 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20211123 N/A ANDA ANDA078069 Bryant Ranch Prepack OXCARBAZEPINE 300 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-0090-5)
63629-2075-1 63629-2075 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20210204 N/A ANDA ANDA078069 Bryant Ranch Prepack OXCARBAZEPINE 300 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (63629-2075-1)
55154-4320-0 55154-4320 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20230801 N/A ANDA ANDA078069 Cardinal Health 107, LLC OXCARBAZEPINE 300 mg/1 10 BLISTER PACK in 1 BAG (55154-4320-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
55154-4323-0 55154-4323 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20230801 N/A ANDA ANDA078069 Cardinal Health 107, LLC OXCARBAZEPINE 150 mg/1 10 BLISTER PACK in 1 BAG (55154-4323-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
71335-0090-2 71335-0090 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20200924 N/A ANDA ANDA078069 Bryant Ranch Prepack OXCARBAZEPINE 300 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0090-2)
71335-0090-1 71335-0090 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20200604 N/A ANDA ANDA078069 Bryant Ranch Prepack OXCARBAZEPINE 300 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0090-1)
71335-0090-4 71335-0090 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20211123 N/A ANDA ANDA078069 Bryant Ranch Prepack OXCARBAZEPINE 300 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71335-0090-4)
55154-8187-0 55154-8187 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20141104 N/A ANDA ANDA078069 Cardinal Health 107, LLC OXCARBAZEPINE 150 mg/1 10 BLISTER PACK in 1 BAG (55154-8187-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
55154-8198-0 55154-8198 HUMAN PRESCRIPTION DRUG Oxcarbazepine Oxcarbazepine TABLET, FILM COATED ORAL 20141105 N/A ANDA ANDA078069 Cardinal Health 107, LLC OXCARBAZEPINE 300 mg/1 10 BLISTER PACK in 1 BAG (55154-8198-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
51991-293-01 51991-293 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20080111 N/A ANDA ANDA078069 Breckenridge Pharmaceutical, Inc. OXCARBAZEPINE 300 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (51991-293-01)
51991-294-01 51991-294 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20080111 N/A ANDA ANDA078069 Breckenridge Pharmaceutical, Inc. OXCARBAZEPINE 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (51991-294-01)
51991-294-05 51991-294 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20080111 N/A ANDA ANDA078069 Breckenridge Pharmaceutical, Inc. OXCARBAZEPINE 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (51991-294-05)
51991-293-05 51991-293 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20080111 N/A ANDA ANDA078069 Breckenridge Pharmaceutical, Inc. OXCARBAZEPINE 300 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (51991-293-05)
51991-292-01 51991-292 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20080111 N/A ANDA ANDA078069 Breckenridge Pharmaceutical, Inc. OXCARBAZEPINE 150 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (51991-292-01)
51991-292-05 51991-292 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20080111 N/A ANDA ANDA078069 Breckenridge Pharmaceutical, Inc. OXCARBAZEPINE 150 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (51991-292-05)
63629-9186-1 63629-9186 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20220803 N/A ANDA ANDA078069 Bryant Ranch Prepack OXCARBAZEPINE 300 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (63629-9186-1)
68788-7866-3 68788-7866 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20210215 N/A ANDA ANDA078069 Preferred Pharmaceuticals Inc. OXCARBAZEPINE 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-7866-3)
63629-3816-1 63629-3816 HUMAN PRESCRIPTION DRUG OXCARBAZEPINE OXCARBAZEPINE TABLET, FILM COATED ORAL 20110728 N/A ANDA ANDA078069 Bryant Ranch Prepack OXCARBAZEPINE 150 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63629-3816-1)
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