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=ANDA210628"
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
70518-3424-2 70518-3424 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20250616 N/A ANDA ANDA210628 REMEDYREPACK INC. CELECOXIB 100 mg/1 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-3424-2)
70518-3424-1 70518-3424 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20250523 N/A ANDA ANDA210628 REMEDYREPACK INC. CELECOXIB 100 mg/1 60 CAPSULE in 1 BOTTLE, PLASTIC (70518-3424-1)
70518-3292-3 70518-3292 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20250305 N/A ANDA ANDA210628 REMEDYREPACK INC. CELECOXIB 200 mg/1 45 CAPSULE in 1 BOTTLE, PLASTIC (70518-3292-3)
71335-2019-1 71335-2019 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20220104 N/A ANDA ANDA210628 Bryant Ranch Prepack CELECOXIB 100 mg/1 30 CAPSULE in 1 BOTTLE (71335-2019-1)
71335-2019-5 71335-2019 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20250130 N/A ANDA ANDA210628 Bryant Ranch Prepack CELECOXIB 100 mg/1 120 CAPSULE in 1 BOTTLE (71335-2019-5)
71335-2019-6 71335-2019 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20250130 N/A ANDA ANDA210628 Bryant Ranch Prepack CELECOXIB 100 mg/1 14 CAPSULE in 1 BOTTLE (71335-2019-6)
71335-2019-7 71335-2019 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20250130 N/A ANDA ANDA210628 Bryant Ranch Prepack CELECOXIB 100 mg/1 10 CAPSULE in 1 BOTTLE (71335-2019-7)
71335-2019-2 71335-2019 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20250130 N/A ANDA ANDA210628 Bryant Ranch Prepack CELECOXIB 100 mg/1 20 CAPSULE in 1 BOTTLE (71335-2019-2)
71335-2019-3 71335-2019 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20220104 N/A ANDA ANDA210628 Bryant Ranch Prepack CELECOXIB 100 mg/1 60 CAPSULE in 1 BOTTLE (71335-2019-3)
71335-2019-4 71335-2019 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20250130 N/A ANDA ANDA210628 Bryant Ranch Prepack CELECOXIB 100 mg/1 90 CAPSULE in 1 BOTTLE (71335-2019-4)
75834-236-05 75834-236 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20200903 N/A ANDA ANDA210628 NIVAGEN PHARMACEUTICALS, INC. CELECOXIB 50 mg/1 500 CAPSULE in 1 BOTTLE (75834-236-05)
75834-237-05 75834-237 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20200903 N/A ANDA ANDA210628 NIVAGEN PHARMACEUTICALS, INC. CELECOXIB 100 mg/1 500 CAPSULE in 1 BOTTLE (75834-237-05)
75834-237-11 75834-237 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20200903 N/A ANDA ANDA210628 NIVAGEN PHARMACEUTICALS, INC. CELECOXIB 100 mg/1 100 CAPSULE in 1 BLISTER PACK (75834-237-11)
75834-238-01 75834-238 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20200903 N/A ANDA ANDA210628 NIVAGEN PHARMACEUTICALS, INC. CELECOXIB 200 mg/1 100 CAPSULE in 1 BOTTLE (75834-238-01)
75834-238-05 75834-238 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20200903 N/A ANDA ANDA210628 NIVAGEN PHARMACEUTICALS, INC. CELECOXIB 200 mg/1 500 CAPSULE in 1 BOTTLE (75834-238-05)
75834-238-11 75834-238 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20200903 N/A ANDA ANDA210628 NIVAGEN PHARMACEUTICALS, INC. CELECOXIB 200 mg/1 100 CAPSULE in 1 BLISTER PACK (75834-238-11)
75834-239-05 75834-239 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20200903 N/A ANDA ANDA210628 NIVAGEN PHARMACEUTICALS, INC. CELECOXIB 400 mg/1 500 CAPSULE in 1 BOTTLE (75834-239-05)
75834-239-11 75834-239 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20200903 N/A ANDA ANDA210628 NIVAGEN PHARMACEUTICALS, INC. CELECOXIB 400 mg/1 100 CAPSULE in 1 BLISTER PACK (75834-239-11)
75834-236-11 75834-236 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20200903 N/A ANDA ANDA210628 NIVAGEN PHARMACEUTICALS, INC. CELECOXIB 50 mg/1 100 CAPSULE in 1 BLISTER PACK (75834-236-11)
75834-236-60 75834-236 HUMAN PRESCRIPTION DRUG CELECOXIB CELECOXIB CAPSULE ORAL 20200903 N/A ANDA ANDA210628 NIVAGEN PHARMACEUTICALS, INC. CELECOXIB 50 mg/1 60 CAPSULE in 1 BOTTLE (75834-236-60)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase