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 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
72189-080-30 72189-080 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20200513 N/A ANDA ANDA208170 DIRECT RX CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-080-30)
72189-080-45 72189-080 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20200513 N/A ANDA ANDA208170 DIRECT RX CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (72189-080-45)
72189-080-60 72189-080 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20200513 N/A ANDA ANDA208170 DIRECT RX CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (72189-080-60)
50090-4729-4 50090-4729 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA208170 A-S Medication Solutions CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 42 TABLET, FILM COATED in 1 BOTTLE (50090-4729-4)
50090-4729-8 50090-4729 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20191118 N/A ANDA ANDA208170 A-S Medication Solutions CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (50090-4729-8)
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)
60760-766-04 60760-766 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230629 N/A ANDA ANDA208170 ST. MARY'S MEDICAL PARK PHARMACY CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-766-04)
60760-766-15 60760-766 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230629 N/A ANDA ANDA208170 ST. MARY'S MEDICAL PARK PHARMACY CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-766-15)
60760-766-30 60760-766 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20170531 N/A ANDA ANDA208170 ST. MARY'S MEDICAL PARK PHARMACY CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-766-30)
60760-766-90 60760-766 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20231101 N/A ANDA ANDA208170 ST. MARY'S MEDICAL PARK PHARMACY CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-766-90)
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)
76420-456-00 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 1000 TABLET, FILM COATED in 1 BOTTLE (76420-456-00)
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)
76420-456-03 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20260403 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (76420-456-03)
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)
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