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=ANDA213324"
符合检索条件的记录共 125 条，共 7 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
50090-5711-3 50090-5711 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20210924 N/A ANDA ANDA213324 A-S Medication Solutions CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-5711-3)
76420-839-00 76420-839 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76420-839-00)
76420-839-01 76420-839 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 1 TABLET, FILM COATED in 1 BOTTLE (76420-839-01)
76420-839-02 76420-839 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 2 TABLET, FILM COATED in 1 BOTTLE (76420-839-02)
76420-839-07 76420-839 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (76420-839-07)
76420-839-30 76420-839 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-839-30)
76420-839-60 76420-839 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-839-60)
76420-839-90 76420-839 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-839-90)
76420-840-00 76420-840 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76420-840-00)
76420-840-01 76420-840 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 1 TABLET, FILM COATED in 1 BOTTLE (76420-840-01)
76420-840-02 76420-840 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 2 TABLET, FILM COATED in 1 BOTTLE (76420-840-02)
76420-839-10 76420-839 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-839-10)
76420-839-20 76420-839 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (76420-839-20)
76420-839-05 76420-839 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-839-05)
76420-840-07 76420-840 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (76420-840-07)
76420-840-60 76420-840 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-840-60)
76420-840-90 76420-840 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-840-90)
76420-841-00 76420-841 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76420-841-00)
76420-841-01 76420-841 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 1 TABLET, FILM COATED in 1 BOTTLE (76420-841-01)
76420-841-02 76420-841 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 2 TABLET, FILM COATED in 1 BOTTLE (76420-841-02)
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