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=ANDA208170"
符合检索条件的记录共 292 条，共 15 页，当前第 10 页 ，可点击列名称排序
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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
71205-065-10 71205-065 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71205-065-10)
71205-065-12 71205-065 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (71205-065-12)
71205-065-15 71205-065 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71205-065-15)
71205-065-20 71205-065 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71205-065-20)
71205-065-21 71205-065 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (71205-065-21)
71205-065-30 71205-065 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-065-30)
71205-065-45 71205-065 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (71205-065-45)
71205-065-60 71205-065 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-065-60)
71205-065-72 71205-065 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71205-065-72)
71205-065-90 71205-065 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-065-90)
72888-013-01 72888-013 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20170531 N/A ANDA ANDA208170 Advagen Pharma Limited CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72888-013-01)
72603-310-01 72603-310 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20241101 N/A ANDA ANDA208170 NORTHSTAR RX LLC CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72603-310-01)
72603-310-02 72603-310 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20241101 N/A ANDA ANDA208170 NORTHSTAR RX LLC CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72603-310-02)
71335-2479-0 71335-2479 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250203 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-2479-0)
71335-2479-1 71335-2479 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240924 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2479-1)
71335-2479-2 71335-2479 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20241108 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-2479-2)
71335-2479-3 71335-2479 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20241008 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (71335-2479-3)
71335-2479-4 71335-2479 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250203 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71335-2479-4)
76420-011-05 76420-011 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20241224 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (76420-011-05)
76420-011-07 76420-011 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20200123 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (76420-011-07)
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