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=ANDA213949"
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
31722-240-30 31722-240 HUMAN PRESCRIPTION DRUG lamotrigine lamotrigine extended-release TABLET, FILM COATED, EXTENDED RELEASE ORAL 20211209 N/A ANDA ANDA213949 Camber Pharmaceuticals Inc LAMOTRIGINE 25 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-240-30)
31722-244-30 31722-244 HUMAN PRESCRIPTION DRUG lamotrigine lamotrigine extended-release TABLET, FILM COATED, EXTENDED RELEASE ORAL 20211209 N/A ANDA ANDA213949 Camber Pharmaceuticals Inc LAMOTRIGINE 250 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-244-30)
31722-242-30 31722-242 HUMAN PRESCRIPTION DRUG lamotrigine lamotrigine extended-release TABLET, FILM COATED, EXTENDED RELEASE ORAL 20211209 N/A ANDA ANDA213949 Camber Pharmaceuticals Inc LAMOTRIGINE 100 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-242-30)
72189-560-30 72189-560 HUMAN PRESCRIPTION DRUG Lamotrigine ER Lamotrigine ER TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240619 N/A ANDA ANDA213949 Direct_rx LAMOTRIGINE 200 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-560-30)
31722-243-30 31722-243 HUMAN PRESCRIPTION DRUG lamotrigine lamotrigine extended-release TABLET, FILM COATED, EXTENDED RELEASE ORAL 20211209 N/A ANDA ANDA213949 Camber Pharmaceuticals Inc LAMOTRIGINE 200 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-243-30)
82804-022-30 82804-022 HUMAN PRESCRIPTION DRUG lamotrigine lamotrigine extended-release TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231011 N/A ANDA ANDA213949 Proficient Rx LP LAMOTRIGINE 50 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82804-022-30)
82804-022-60 82804-022 HUMAN PRESCRIPTION DRUG lamotrigine lamotrigine extended-release TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231011 N/A ANDA ANDA213949 Proficient Rx LP LAMOTRIGINE 50 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82804-022-60)
82804-022-90 82804-022 HUMAN PRESCRIPTION DRUG lamotrigine lamotrigine extended-release TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231011 N/A ANDA ANDA213949 Proficient Rx LP LAMOTRIGINE 50 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82804-022-90)
31722-241-30 31722-241 HUMAN PRESCRIPTION DRUG lamotrigine lamotrigine extended-release TABLET, FILM COATED, EXTENDED RELEASE ORAL 20211209 N/A ANDA ANDA213949 Camber Pharmaceuticals Inc LAMOTRIGINE 50 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-241-30)
31722-245-30 31722-245 HUMAN PRESCRIPTION DRUG lamotrigine lamotrigine extended-release TABLET, FILM COATED, EXTENDED RELEASE ORAL 20211209 N/A ANDA ANDA213949 Camber Pharmaceuticals Inc LAMOTRIGINE 300 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-245-30)
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