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=ANDA090170"
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
71335-0830-1 71335-0830 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20220209 N/A ANDA ANDA090170 Bryant Ranch Prepack LAMOTRIGINE 200 mg/1 30 TABLET in 1 BOTTLE (71335-0830-1)
71335-0830-5 71335-0830 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20220209 N/A ANDA ANDA090170 Bryant Ranch Prepack LAMOTRIGINE 200 mg/1 180 TABLET in 1 BOTTLE (71335-0830-5)
71335-0830-6 71335-0830 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20220209 N/A ANDA ANDA090170 Bryant Ranch Prepack LAMOTRIGINE 200 mg/1 14 TABLET in 1 BOTTLE (71335-0830-6)
71335-0830-2 71335-0830 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20220209 N/A ANDA ANDA090170 Bryant Ranch Prepack LAMOTRIGINE 200 mg/1 60 TABLET in 1 BOTTLE (71335-0830-2)
71335-0830-3 71335-0830 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20220209 N/A ANDA ANDA090170 Bryant Ranch Prepack LAMOTRIGINE 200 mg/1 90 TABLET in 1 BOTTLE (71335-0830-3)
71335-0830-4 71335-0830 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20220209 N/A ANDA ANDA090170 Bryant Ranch Prepack LAMOTRIGINE 200 mg/1 45 TABLET in 1 BOTTLE (71335-0830-4)
51655-719-52 51655-719 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20210614 N/A ANDA ANDA090170 Northwind Pharmaceuticals LAMOTRIGINE 25 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-719-52)
53002-2513-3 53002-2513 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20200101 N/A ANDA ANDA090170 RPK Pharmaceuticals, Inc. LAMOTRIGINE 25 mg/1 30 TABLET in 1 BOTTLE (53002-2513-3)
53002-2512-0 53002-2512 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20190101 N/A ANDA ANDA090170 RPK Pharmaceuticals, Inc. LAMOTRIGINE 100 mg/1 100 TABLET in 1 BOTTLE (53002-2512-0)
53002-2512-3 53002-2512 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20190101 N/A ANDA ANDA090170 RPK Pharmaceuticals, Inc. LAMOTRIGINE 100 mg/1 30 TABLET in 1 BOTTLE (53002-2512-3)
53002-2513-0 53002-2513 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20200101 N/A ANDA ANDA090170 RPK Pharmaceuticals, Inc. LAMOTRIGINE 25 mg/1 100 TABLET in 1 BOTTLE (53002-2513-0)
55700-626-60 55700-626 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20180706 N/A ANDA ANDA090170 Lake Erie Medical DBA Quality Care Products LLC LAMOTRIGINE 100 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (55700-626-60)
55700-683-30 55700-683 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20180914 N/A ANDA ANDA090170 Lake Erie Medical DBA Quality Care Products LLC LAMOTRIGINE 25 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (55700-683-30)
55700-683-60 55700-683 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20180914 N/A ANDA ANDA090170 Lake Erie Medical DBA Quality Care Products LLC LAMOTRIGINE 25 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (55700-683-60)
61919-534-60 61919-534 HUMAN PRESCRIPTION DRUG LAMOTRIGINE LAMOTRIGINE TABLET ORAL 20220725 N/A ANDA ANDA090170 DirectRX LAMOTRIGINE 100 mg/1 60 TABLET in 1 BOTTLE (61919-534-60)
61919-534-30 61919-534 HUMAN PRESCRIPTION DRUG LAMOTRIGINE LAMOTRIGINE TABLET ORAL 20190417 N/A ANDA ANDA090170 DirectRX LAMOTRIGINE 100 mg/1 30 TABLET in 1 BOTTLE (61919-534-30)
68071-2054-4 68071-2054 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20220519 N/A ANDA ANDA090170 NuCare Pharmaceuticals,Inc. LAMOTRIGINE 25 mg/1 42 TABLET in 1 BOTTLE, PLASTIC (68071-2054-4)
68071-2054-9 68071-2054 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20220519 N/A ANDA ANDA090170 NuCare Pharmaceuticals,Inc. LAMOTRIGINE 25 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (68071-2054-9)
71205-245-30 71205-245 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20190401 N/A ANDA ANDA090170 Proficient Rx LP LAMOTRIGINE 100 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (71205-245-30)
71205-245-90 71205-245 HUMAN PRESCRIPTION DRUG Lamotrigine Lamotrigine TABLET ORAL 20190401 N/A ANDA ANDA090170 Proficient Rx LP LAMOTRIGINE 100 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (71205-245-90)
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