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=NDA020699"
符合检索条件的记录共 18 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
71610-018-79 71610-018 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 20171212 N/A NDA AUTHORIZED GENERIC NDA020699 Aphena Pharma Solutions - Tennessee, LLC VENLAFAXINE HYDROCHLORIDE 75 mg/1 2160 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71610-018-79)
58151-125-77 58151-125 HUMAN PRESCRIPTION DRUG Effexor XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 20240717 N/A NDA NDA020699 Viatris Specialty LLC VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-125-77)
58151-125-93 58151-125 HUMAN PRESCRIPTION DRUG Effexor XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 20240717 N/A NDA NDA020699 Viatris Specialty LLC VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-125-93)
45865-643-30 45865-643 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20150911 N/A NDA AUTHORIZED GENERIC NDA020699 Medsource Pharmaceuticals VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (45865-643-30)
45865-643-60 45865-643 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20150911 N/A NDA AUTHORIZED GENERIC NDA020699 Medsource Pharmaceuticals VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (45865-643-60)
0008-0836-21 0008-0836 HUMAN PRESCRIPTION DRUG Effexor XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 19971101 N/A NDA NDA020699 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0008-0836-21)
0008-0836-22 0008-0836 HUMAN PRESCRIPTION DRUG Effexor XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 19971101 20250531 NDA NDA020699 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0008-0836-22)
58151-127-77 58151-127 HUMAN PRESCRIPTION DRUG Effexor XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 20240801 N/A NDA NDA020699 Viatris Specialty LLC VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-127-77)
45865-647-30 45865-647 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20150911 N/A NDA AUTHORIZED GENERIC NDA020699 Medsource Pharmaceuticals VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (45865-647-30)
45865-647-60 45865-647 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20150911 N/A NDA AUTHORIZED GENERIC NDA020699 Medsource Pharmaceuticals VENLAFAXINE HYDROCHLORIDE 75 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (45865-647-60)
0008-0837-21 0008-0837 HUMAN PRESCRIPTION DRUG Effexor XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 19971101 20250531 NDA NDA020699 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0008-0837-21)
0008-0837-22 0008-0837 HUMAN PRESCRIPTION DRUG Effexor XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 19971101 20250531 NDA NDA020699 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0008-0837-22)
71610-013-53 71610-013 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 20171201 N/A NDA AUTHORIZED GENERIC NDA020699 Aphena Pharma Solutions - Tennessee, LLC VENLAFAXINE HYDROCHLORIDE 150 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71610-013-53)
71610-013-79 71610-013 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 20171205 N/A NDA AUTHORIZED GENERIC NDA020699 Aphena Pharma Solutions - Tennessee, LLC VENLAFAXINE HYDROCHLORIDE 150 mg/1 2160 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71610-013-79)
0008-0833-21 0008-0833 HUMAN PRESCRIPTION DRUG Effexor XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 19971101 20251031 NDA NDA020699 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0008-0833-21)
0008-0833-22 0008-0833 HUMAN PRESCRIPTION DRUG Effexor XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 19971101 20251031 NDA NDA020699 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0008-0833-22)
58151-126-77 58151-126 HUMAN PRESCRIPTION DRUG Effexor XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 20241030 N/A NDA NDA020699 Viatris Specialty LLC VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-126-77)
58151-126-93 58151-126 HUMAN PRESCRIPTION DRUG Effexor XR VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE ORAL 20241030 N/A NDA NDA020699 Viatris Specialty LLC VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-126-93)
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