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 300 条，共 15 页，当前第 4 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
70518-3415-6 70518-3415 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240924 N/A ANDA ANDA208170 REMEDYREPACK INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3415-6)
70518-3415-1 70518-3415 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240430 N/A ANDA ANDA208170 REMEDYREPACK INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3415-1)
70518-3415-5 70518-3415 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240918 N/A ANDA ANDA208170 REMEDYREPACK INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3415-5)
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)
76420-828-12 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/1 120 TABLET, FILM COATED in 1 BOTTLE (76420-828-12)
76420-828-30 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 30 TABLET, FILM COATED in 1 BOTTLE (76420-828-30)
76420-828-60 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 60 TABLET, FILM COATED in 1 BOTTLE (76420-828-60)
76420-828-90 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 90 TABLET, FILM COATED in 1 BOTTLE (76420-828-90)
76420-829-01 76420-829 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240702 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-829-01)
76420-829-07 76420-829 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250204 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (76420-829-07)
76420-829-12 76420-829 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240702 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (76420-829-12)
76420-829-30 76420-829 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240702 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-829-30)
76420-829-60 76420-829 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240702 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-829-60)
76420-829-90 76420-829 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240702 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-829-90)
76420-830-00 76420-830 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240702 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76420-830-00)
76420-830-01 76420-830 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240702 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-830-01)
76420-830-05 76420-830 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240702 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-830-05)
76420-830-07 76420-830 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240702 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (76420-830-07)
76420-830-12 76420-830 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240702 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (76420-830-12)
76420-830-30 76420-830 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240702 N/A ANDA ANDA208170 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-830-30)
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