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=ANDA205468"
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
29033-046-30 29033-046 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride venlafaxine hydrochloride TABLET, EXTENDED RELEASE ORAL 20170327 N/A ANDA ANDA205468 Nostrum Laboratories, Inc. VENLAFAXINE HYDROCHLORIDE 225 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (29033-046-30)
29033-046-90 29033-046 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride venlafaxine hydrochloride TABLET, EXTENDED RELEASE ORAL 20170327 N/A ANDA ANDA205468 Nostrum Laboratories, Inc. VENLAFAXINE HYDROCHLORIDE 225 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (29033-046-90)
29033-045-30 29033-045 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride venlafaxine hydrochloride TABLET, EXTENDED RELEASE ORAL 20170327 N/A ANDA ANDA205468 Nostrum Laboratories, Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (29033-045-30)
29033-045-90 29033-045 HUMAN PRESCRIPTION DRUG Venlafaxine Hydrochloride venlafaxine hydrochloride TABLET, EXTENDED RELEASE ORAL 20170327 N/A ANDA ANDA205468 Nostrum Laboratories, Inc. VENLAFAXINE HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (29033-045-90)
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