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=ANDA090165"
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
76483-103-01 76483-103 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET, ORALLY DISINTEGRATING ORAL 20220720 N/A ANDA ANDA090165 SQUARE PHARMACEUTICALS LIMITED ARIPIPRAZOLE 30 mg/1 60 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (76483-103-01)
76483-103-02 76483-103 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET, ORALLY DISINTEGRATING ORAL 20220720 N/A ANDA ANDA090165 SQUARE PHARMACEUTICALS LIMITED ARIPIPRAZOLE 30 mg/1 90 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (76483-103-02)
72578-107-06 72578-107 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET, ORALLY DISINTEGRATING ORAL 20220720 N/A ANDA ANDA090165 Viona Pharmaceuticals Inc. ARIPIPRAZOLE 15 mg/1 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (72578-107-06)
72578-107-78 72578-107 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET, ORALLY DISINTEGRATING ORAL 20230222 N/A ANDA ANDA090165 Viona Pharmaceuticals Inc. ARIPIPRAZOLE 15 mg/1 3 BLISTER PACK in 1 CARTON (72578-107-78) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (72578-107-30)
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