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=ANDA208212"
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
0480-2045-56 0480-2045 HUMAN PRESCRIPTION DRUG Vilazodone Hydrochloride Vilazodone Hydrochloride TABLET, FILM COATED ORAL 20220606 N/A ANDA ANDA208212 Teva Pharmaceuticals, Inc. VILAZODONE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0480-2045-56)
0480-2044-56 0480-2044 HUMAN PRESCRIPTION DRUG Vilazodone Hydrochloride Vilazodone Hydrochloride TABLET, FILM COATED ORAL 20220606 N/A ANDA ANDA208212 Teva Pharmaceuticals, Inc. VILAZODONE HYDROCHLORIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0480-2044-56)
0480-2043-56 0480-2043 HUMAN PRESCRIPTION DRUG Vilazodone Hydrochloride Vilazodone Hydrochloride TABLET, FILM COATED ORAL 20220606 N/A ANDA ANDA208212 Teva Pharmaceuticals, Inc. VILAZODONE HYDROCHLORIDE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0480-2043-56)
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