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
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)
68788-8197-1 68788-8197 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20220523 N/A ANDA ANDA205129 Preferred Pharmaceuticals, Inc. CELECOXIB 200 mg/1 100 CAPSULE in 1 BOTTLE (68788-8197-1)
68788-8197-3 68788-8197 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20220523 N/A ANDA ANDA205129 Preferred Pharmaceuticals, Inc. CELECOXIB 200 mg/1 30 CAPSULE in 1 BOTTLE (68788-8197-3)
68788-8197-6 68788-8197 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20220523 N/A ANDA ANDA205129 Preferred Pharmaceuticals, Inc. CELECOXIB 200 mg/1 60 CAPSULE in 1 BOTTLE (68788-8197-6)
68788-8197-8 68788-8197 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20220523 N/A ANDA ANDA205129 Preferred Pharmaceuticals, Inc. CELECOXIB 200 mg/1 120 CAPSULE in 1 BOTTLE (68788-8197-8)
68788-8197-9 68788-8197 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20220523 N/A ANDA ANDA205129 Preferred Pharmaceuticals, Inc. CELECOXIB 200 mg/1 90 CAPSULE in 1 BOTTLE (68788-8197-9)
72162-2175-3 72162-2175 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20231207 N/A ANDA ANDA205129 Bryant Ranch Prepack CELECOXIB 200 mg/1 30 CAPSULE in 1 BOTTLE (72162-2175-3)
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)
72789-259-60 72789-259 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20220920 N/A ANDA ANDA205129 PD-Rx Pharmaceuticals, Inc. CELECOXIB 200 mg/1 60 CAPSULE in 1 BOTTLE, PLASTIC (72789-259-60)
71205-664-14 71205-664 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20230427 N/A ANDA ANDA205129 Proficient Rx LP CELECOXIB 200 mg/1 14 CAPSULE in 1 BOTTLE (71205-664-14)
71205-664-30 71205-664 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20220525 N/A ANDA ANDA205129 Proficient Rx LP CELECOXIB 200 mg/1 30 CAPSULE in 1 BOTTLE (71205-664-30)
71205-664-60 71205-664 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20220525 N/A ANDA ANDA205129 Proficient Rx LP CELECOXIB 200 mg/1 60 CAPSULE in 1 BOTTLE (71205-664-60)
71205-664-90 71205-664 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20220525 N/A ANDA ANDA205129 Proficient Rx LP CELECOXIB 200 mg/1 90 CAPSULE in 1 BOTTLE (71205-664-90)
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)
70518-4619-0 70518-4619 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20260424 N/A ANDA ANDA205129 REMEDYREPACK INC. CELECOXIB 400 mg/1 50 POUCH in 1 BOX (70518-4619-0) / 1 CAPSULE in 1 POUCH (70518-4619-1)
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)
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