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=ANDA205129"
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
72162-2175-5 72162-2175 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20231207 N/A ANDA ANDA205129 Bryant Ranch Prepack CELECOXIB 200 mg/1 500 CAPSULE in 1 BOTTLE (72162-2175-5)
72162-2175-6 72162-2175 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20231207 N/A ANDA ANDA205129 Bryant Ranch Prepack CELECOXIB 200 mg/1 60 CAPSULE in 1 BOTTLE (72162-2175-6)
72162-2254-5 72162-2254 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20240223 N/A ANDA ANDA205129 Bryant Ranch Prepack CELECOXIB 100 mg/1 500 CAPSULE in 1 BOTTLE (72162-2254-5)
77771-156-60 77771-156 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20210415 N/A ANDA ANDA205129 Radha Pharmaceuticals, Inc. CELECOXIB 50 mg/1 60 CAPSULE in 1 BOTTLE (77771-156-60)
77771-157-01 77771-157 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20210415 N/A ANDA ANDA205129 Radha Pharmaceuticals, Inc. CELECOXIB 100 mg/1 100 CAPSULE in 1 BOTTLE (77771-157-01)
77771-157-05 77771-157 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20210415 N/A ANDA ANDA205129 Radha Pharmaceuticals, Inc. CELECOXIB 100 mg/1 500 CAPSULE in 1 BOTTLE (77771-157-05)
50228-156-10 50228-156 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20201203 N/A ANDA ANDA205129 ScieGen Pharmaceuticals, Inc. CELECOXIB 50 mg/1 1000 CAPSULE in 1 BOTTLE (50228-156-10)
50228-156-30 50228-156 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20201203 N/A ANDA ANDA205129 ScieGen Pharmaceuticals, Inc. CELECOXIB 50 mg/1 30 CAPSULE in 1 BOTTLE (50228-156-30)
50228-156-60 50228-156 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20201203 N/A ANDA ANDA205129 ScieGen Pharmaceuticals, Inc. CELECOXIB 50 mg/1 60 CAPSULE in 1 BOTTLE (50228-156-60)
50228-157-01 50228-157 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20201203 N/A ANDA ANDA205129 ScieGen Pharmaceuticals, Inc. CELECOXIB 100 mg/1 100 CAPSULE in 1 BOTTLE (50228-157-01)
50228-157-05 50228-157 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20201203 N/A ANDA ANDA205129 ScieGen Pharmaceuticals, Inc. CELECOXIB 100 mg/1 500 CAPSULE in 1 BOTTLE (50228-157-05)
50228-157-10 50228-157 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20201203 N/A ANDA ANDA205129 ScieGen Pharmaceuticals, Inc. CELECOXIB 100 mg/1 1000 CAPSULE in 1 BOTTLE (50228-157-10)
50228-157-30 50228-157 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20201203 N/A ANDA ANDA205129 ScieGen Pharmaceuticals, Inc. CELECOXIB 100 mg/1 30 CAPSULE in 1 BOTTLE (50228-157-30)
50228-158-01 50228-158 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20201203 N/A ANDA ANDA205129 ScieGen Pharmaceuticals, Inc. CELECOXIB 200 mg/1 100 CAPSULE in 1 BOTTLE (50228-158-01)
50228-158-05 50228-158 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20201203 N/A ANDA ANDA205129 ScieGen Pharmaceuticals, Inc. CELECOXIB 200 mg/1 500 CAPSULE in 1 BOTTLE (50228-158-05)
50228-158-10 50228-158 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20201203 N/A ANDA ANDA205129 ScieGen Pharmaceuticals, Inc. CELECOXIB 200 mg/1 1000 CAPSULE in 1 BOTTLE (50228-158-10)
50228-158-30 50228-158 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20201203 N/A ANDA ANDA205129 ScieGen Pharmaceuticals, Inc. CELECOXIB 200 mg/1 30 CAPSULE in 1 BOTTLE (50228-158-30)
50228-159-05 50228-159 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20201203 N/A ANDA ANDA205129 ScieGen Pharmaceuticals, Inc. CELECOXIB 400 mg/1 500 CAPSULE in 1 BOTTLE (50228-159-05)
50228-159-30 50228-159 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20201203 N/A ANDA ANDA205129 ScieGen Pharmaceuticals, Inc. CELECOXIB 400 mg/1 30 CAPSULE in 1 BOTTLE (50228-159-30)
50228-159-60 50228-159 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20201203 N/A ANDA ANDA205129 ScieGen Pharmaceuticals, Inc. CELECOXIB 400 mg/1 60 CAPSULE in 1 BOTTLE (50228-159-60)
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