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=ANDA078932"
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
46708-431-31 46708-431 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine TABLET ORAL 20151001 N/A ANDA ANDA078932 Alembic Pharmaceuticals Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 TABLET in 1 BOTTLE (46708-431-31)
46708-431-91 46708-431 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine TABLET ORAL 20151001 N/A ANDA ANDA078932 Alembic Pharmaceuticals Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 1000 TABLET in 1 BOTTLE (46708-431-91)
60760-713-30 60760-713 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine TABLET ORAL 20180927 N/A ANDA ANDA078932 St. Mary's Medical Park Pharmacy VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (60760-713-30)
50090-4715-0 50090-4715 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine TABLET ORAL 20191112 N/A ANDA ANDA078932 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE (50090-4715-0)
50090-4715-1 50090-4715 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine TABLET ORAL 20191112 N/A ANDA ANDA078932 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 TABLET in 1 BOTTLE (50090-4715-1)
51655-332-52 51655-332 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine TABLET ORAL 20210610 N/A ANDA ANDA078932 Northwind Pharmaceuticals, LLC VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-332-52)
62332-008-30 62332-008 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine TABLET ORAL 20151001 N/A ANDA ANDA078932 Alembic Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE (62332-008-30)
62332-008-31 62332-008 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine TABLET ORAL 20151001 N/A ANDA ANDA078932 Alembic Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (62332-008-31)
62332-008-91 62332-008 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine TABLET ORAL 20151001 N/A ANDA ANDA078932 Alembic Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 25 mg/1 1000 TABLET in 1 BOTTLE (62332-008-91)
62332-012-30 62332-012 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine TABLET ORAL 20151001 N/A ANDA ANDA078932 Alembic Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 100 mg/1 30 TABLET in 1 BOTTLE (62332-012-30)
62332-012-31 62332-012 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine TABLET ORAL 20151001 N/A ANDA ANDA078932 Alembic Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (62332-012-31)
62332-012-91 62332-012 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine TABLET ORAL 20151001 N/A ANDA ANDA078932 Alembic Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 100 mg/1 1000 TABLET in 1 BOTTLE (62332-012-91)
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