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=ANDA202700"
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
46708-386-90 46708-386 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Limited MODAFINIL 200 mg/1 90 TABLET in 1 BOTTLE (46708-386-90)
46708-386-91 46708-386 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Limited MODAFINIL 200 mg/1 1000 TABLET in 1 BOTTLE (46708-386-91)
46708-385-10 46708-385 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Limited MODAFINIL 100 mg/1 100 TABLET in 1 CARTON (46708-385-10)
46708-385-30 46708-385 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Limited MODAFINIL 100 mg/1 30 TABLET in 1 BOTTLE (46708-385-30)
46708-385-60 46708-385 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Limited MODAFINIL 100 mg/1 60 TABLET in 1 BOTTLE (46708-385-60)
46708-385-90 46708-385 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Limited MODAFINIL 100 mg/1 90 TABLET in 1 BOTTLE (46708-385-90)
46708-385-91 46708-385 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Limited MODAFINIL 100 mg/1 1000 TABLET in 1 BOTTLE (46708-385-91)
46708-386-60 46708-386 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Limited MODAFINIL 200 mg/1 60 TABLET in 1 BOTTLE (46708-386-60)
46708-386-30 46708-386 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Limited MODAFINIL 200 mg/1 30 TABLET in 1 BOTTLE (46708-386-30)
46708-386-10 46708-386 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Limited MODAFINIL 200 mg/1 100 TABLET in 1 CARTON (46708-386-10)
62332-386-10 62332-386 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Inc. MODAFINIL 200 mg/1 100 TABLET in 1 CARTON (62332-386-10)
62332-386-91 62332-386 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Inc. MODAFINIL 200 mg/1 1000 TABLET in 1 BOTTLE (62332-386-91)
62332-385-60 62332-385 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Inc. MODAFINIL 100 mg/1 60 TABLET in 1 BOTTLE (62332-385-60)
62332-385-90 62332-385 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Inc. MODAFINIL 100 mg/1 90 TABLET in 1 BOTTLE (62332-385-90)
62332-385-91 62332-385 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Inc. MODAFINIL 100 mg/1 1000 TABLET in 1 BOTTLE (62332-385-91)
62332-386-30 62332-386 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Inc. MODAFINIL 200 mg/1 30 TABLET in 1 BOTTLE (62332-386-30)
62332-386-60 62332-386 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Inc. MODAFINIL 200 mg/1 60 TABLET in 1 BOTTLE (62332-386-60)
62332-386-90 62332-386 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Inc. MODAFINIL 200 mg/1 90 TABLET in 1 BOTTLE (62332-386-90)
62332-385-10 62332-385 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Inc. MODAFINIL 100 mg/1 100 TABLET in 1 CARTON (62332-385-10)
62332-385-30 62332-385 HUMAN PRESCRIPTION DRUG Modafinil Modafinil TABLET ORAL 20170630 N/A ANDA ANDA202700 Alembic Pharmaceuticals Inc. MODAFINIL 100 mg/1 30 TABLET in 1 BOTTLE (62332-385-30)
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