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=ANDA090174"
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
68788-8774-2 68788-8774 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20241120 N/A ANDA ANDA090174 Preferred Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 20 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-2)
68788-8774-3 68788-8774 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20241120 N/A ANDA ANDA090174 Preferred Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-3)
68788-8774-6 68788-8774 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20241120 N/A ANDA ANDA090174 Preferred Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-6)
68788-8774-8 68788-8774 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20241120 N/A ANDA ANDA090174 Preferred Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-8)
68788-8774-9 68788-8774 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20241120 N/A ANDA ANDA090174 Preferred Pharmaceuticals Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8774-9)
68071-4442-9 68071-4442 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20180521 N/A ANDA ANDA090174 NuCare Pharmaceuticals,Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-4442-9)
50090-6301-0 50090-6301 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20221229 N/A ANDA ANDA090174 A-S Medication Solutions VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 33 BLISTER PACK in 1 CARTON (50090-6301-0) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase