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
71335-1338-2 71335-1338 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20220209 N/A ANDA ANDA090174 Bryant Ranch Prepack VENLAFAXINE HYDROCHLORIDE 75 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1338-2)
70518-0558-0 70518-0558 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20170530 N/A ANDA ANDA090174 REMEDYREPACK INC. VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-0558-0)
70771-1836-5 70771-1836 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1836-5)
70771-1836-9 70771-1836 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1836-9)
70771-1837-0 70771-1837 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1837-0)
70771-1837-3 70771-1837 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1837-3)
70771-1837-4 70771-1837 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 10 BLISTER PACK in 1 CARTON (70771-1837-4) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70771-1837-2)
70771-1837-5 70771-1837 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1837-5)
70771-1837-9 70771-1837 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 75 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1837-9)
70771-1838-0 70771-1838 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 150 mg/1 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1838-0)
70771-1838-3 70771-1838 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1838-3)
70771-1838-4 70771-1838 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 150 mg/1 10 BLISTER PACK in 1 CARTON (70771-1838-4) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70771-1838-2)
70771-1838-5 70771-1838 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 150 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1838-5)
70771-1838-9 70771-1838 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1838-9)
70771-1836-0 70771-1836 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1836-0)
70771-1836-3 70771-1836 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1836-3)
70771-1836-4 70771-1836 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride Venlafaxine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20230518 N/A ANDA ANDA090174 Zydus Lifesciences Limited VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 10 BLISTER PACK in 1 CARTON (70771-1836-4) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70771-1836-2)
55700-813-30 55700-813 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20191011 N/A ANDA ANDA090174 Quality Care Products, LLC VENLAFAXINE HYDROCHLORIDE 75 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55700-813-30)
55700-813-60 55700-813 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20191011 N/A ANDA ANDA090174 Quality Care Products, LLC VENLAFAXINE HYDROCHLORIDE 75 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55700-813-60)
0904-7075-61 0904-7075 HUMAN PRESCRIPTION DRUG venlafaxine hydrochloride venlafaxine hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20110601 N/A ANDA ANDA090174 Major Pharmaceuticals VENLAFAXINE HYDROCHLORIDE 37.5 mg/1 100 BLISTER PACK in 1 CARTON (0904-7075-61) / 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
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase