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=ANDA090555"
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
60760-304-30 60760-304 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20200616 N/A ANDA ANDA090555 St. Mary's Medical Park Pharmacy VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (60760-304-30)
57237-172-01 57237-172 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (57237-172-01)
57237-172-90 57237-172 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 25 mg/1 90 TABLET in 1 BOTTLE (57237-172-90)
57237-173-01 57237-173 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 TABLET in 1 BOTTLE (57237-173-01)
57237-173-90 57237-173 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 TABLET in 1 BOTTLE (57237-173-90)
57237-174-01 57237-174 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 50 mg/1 100 TABLET in 1 BOTTLE (57237-174-01)
57237-174-90 57237-174 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 50 mg/1 90 TABLET in 1 BOTTLE (57237-174-90)
57237-175-01 57237-175 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 100 TABLET in 1 BOTTLE (57237-175-01)
57237-175-90 57237-175 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 TABLET in 1 BOTTLE (57237-175-90)
57237-176-01 57237-176 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 100 mg/1 100 TABLET in 1 BOTTLE (57237-176-01)
57237-176-90 57237-176 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20100407 N/A ANDA ANDA090555 Rising Pharma Holdings, Inc. VENLAFAXINE HYDROCHLORIDE 100 mg/1 90 TABLET in 1 BOTTLE (57237-176-90)
71335-1213-4 71335-1213 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20220209 N/A ANDA ANDA090555 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 10 TABLET in 1 BOTTLE (71335-1213-4)
51655-223-26 51655-223 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20230227 N/A ANDA ANDA090555 Northwind Pharmaceuticals, LLC VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (51655-223-26)
51655-223-52 51655-223 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20221025 N/A ANDA ANDA090555 Northwind Pharmaceuticals, LLC VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-223-52)
51655-323-52 51655-323 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20230502 N/A ANDA ANDA090555 Northwind Pharmaceuticals, LLC VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-323-52)
50090-4853-0 50090-4853 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20200120 N/A ANDA ANDA090555 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 TABLET in 1 BOTTLE (50090-4853-0)
50090-4853-1 50090-4853 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20200120 N/A ANDA ANDA090555 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 TABLET in 1 BOTTLE (50090-4853-1)
55700-816-90 55700-816 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20191108 N/A ANDA ANDA090555 Quality Care Products, LLC VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 TABLET in 1 BOTTLE (55700-816-90)
70518-1385-0 70518-1385 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20180824 N/A ANDA ANDA090555 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 TABLET in 1 BLISTER PACK (70518-1385-0)
70518-1385-1 70518-1385 HUMAN PRESCRIPTION DRUG venlafaxine venlafaxine hydrochloride TABLET ORAL 20181004 N/A ANDA ANDA090555 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (70518-1385-1)
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