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"
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
76420-840-00 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)
76420-840-07 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)
76420-840-10 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/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-840-10)
70518-3702-1 70518-3702 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230412 N/A ANDA ANDA213324 REMEDYREPACK INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3702-1)
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)
76420-839-05 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)
76420-839-07 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)
76420-839-10 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)
76420-839-30 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)
72189-280-15 72189-280 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20211007 N/A ANDA ANDA213324 DirectRx CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (72189-280-15)
72189-280-20 72189-280 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20211007 N/A ANDA ANDA213324 DirectRx CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (72189-280-20)
72189-280-30 72189-280 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20211007 N/A ANDA ANDA213324 DirectRx CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-280-30)
72189-280-60 72189-280 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20211007 N/A ANDA ANDA213324 DirectRx CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (72189-280-60)
72189-280-82 72189-280 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20211007 N/A ANDA ANDA213324 DirectRx CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (72189-280-82)
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