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 7 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
71335-1266-3 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1266-3)
71335-1266-4 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-1266-4)
71335-1266-5 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-1266-5)
71335-1266-6 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1266-6)
71335-1266-7 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1266-7)
71335-1266-8 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 56 TABLET, FILM COATED in 1 BOTTLE (71335-1266-8)
71335-1266-9 71335-1266 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA208170 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-1266-9)
52817-332-00 52817-332 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20170531 N/A ANDA ANDA208170 TruPharma LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (52817-332-00)
52817-332-10 52817-332 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20170531 N/A ANDA ANDA208170 TruPharma LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (52817-332-10)
52817-332-50 52817-332 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20170531 N/A ANDA ANDA208170 TruPharma LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (52817-332-50)
51655-592-20 51655-592 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230131 N/A ANDA ANDA208170 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-20)
51655-592-25 51655-592 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230502 N/A ANDA ANDA208170 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-25)
51655-592-26 51655-592 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230207 N/A ANDA ANDA208170 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-26)
51655-592-52 51655-592 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230103 N/A ANDA ANDA208170 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-52)
51655-592-53 51655-592 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230103 N/A ANDA ANDA208170 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-53)
51655-592-54 51655-592 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230103 N/A ANDA ANDA208170 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-54)
76420-828-00 76420-828 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240702 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76420-828-00)
76420-828-01 76420-828 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240702 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-828-01)
76420-828-05 76420-828 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240702 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-828-05)
76420-828-07 76420-828 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250204 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (76420-828-07)
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