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=ANDA078643"
符合检索条件的记录共 85 条，共 5 页，当前第 3 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
16571-783-10 16571-783 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20080926 N/A ANDA ANDA078643 Rising Pharma Holdings, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16571-783-10)
16571-783-50 16571-783 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20080926 N/A ANDA ANDA078643 Rising Pharma Holdings, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (16571-783-50)
65862-190-01 65862-190 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20080926 N/A ANDA ANDA078643 Aurobindo Pharma Limited CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-190-01)
65862-190-05 65862-190 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20080926 N/A ANDA ANDA078643 Aurobindo Pharma Limited CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-190-05)
65862-190-99 65862-190 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20080926 N/A ANDA ANDA078643 Aurobindo Pharma Limited CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-190-99)
71335-2678-1 71335-2678 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20250911 N/A ANDA ANDA078643 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (71335-2678-1)
16571-782-01 16571-782 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20080926 N/A ANDA ANDA078643 Rising Pharma Holdings, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16571-782-01)
16571-782-10 16571-782 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20080926 N/A ANDA ANDA078643 Rising Pharma Holdings, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16571-782-10)
16571-782-50 16571-782 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20080926 N/A ANDA ANDA078643 Rising Pharma Holdings, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (16571-782-50)
71335-2156-5 71335-2156 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220822 N/A ANDA ANDA078643 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-2156-5)
71335-2156-6 71335-2156 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220822 N/A ANDA ANDA078643 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71335-2156-6)
42708-172-20 42708-172 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230519 N/A ANDA ANDA078643 QPharma Inc CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-172-20)
71335-2156-7 71335-2156 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220822 N/A ANDA ANDA078643 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-2156-7)
71335-2156-8 71335-2156 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220822 N/A ANDA ANDA078643 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-2156-8)
71335-2156-9 71335-2156 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220822 N/A ANDA ANDA078643 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-2156-9)
65862-191-01 65862-191 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20080926 N/A ANDA ANDA078643 Aurobindo Pharma Limited CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-191-01)
65862-191-05 65862-191 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20080926 N/A ANDA ANDA078643 Aurobindo Pharma Limited CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-191-05)
65862-191-99 65862-191 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20080926 N/A ANDA ANDA078643 Aurobindo Pharma Limited CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-191-99)
0904-7400-04 0904-7400 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20240221 20270131 ANDA ANDA078643 Major Pharmaceuticals CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 BLISTER PACK in 1 CARTON (0904-7400-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-7400-06 0904-7400 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20240221 20270131 ANDA ANDA078643 Major Pharmaceuticals CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 50 BLISTER PACK in 1 CARTON (0904-7400-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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