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 294 条，共 15 页，当前第 2 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
76420-456-01 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 1 TABLET, FILM COATED in 1 BOTTLE (76420-456-01)
76420-456-02 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 2 TABLET, FILM COATED in 1 BOTTLE (76420-456-02)
76420-456-04 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (76420-456-04)
76420-456-05 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (76420-456-05)
76420-456-07 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (76420-456-07)
76420-456-10 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-456-10)
76420-456-14 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (76420-456-14)
76420-456-15 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (76420-456-15)
76420-456-20 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (76420-456-20)
76420-456-30 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-456-30)
76420-456-50 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-456-50)
76420-456-60 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-456-60)
76420-456-90 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-456-90)
51655-539-20 51655-539 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20210114 N/A ANDA ANDA208170 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-20)
51655-539-52 51655-539 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20210526 N/A ANDA ANDA208170 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-52)
51655-539-53 51655-539 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20220415 N/A ANDA ANDA208170 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-53)
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)
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