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=ANDA078643"
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
45865-244-14 45865-244 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230307 N/A ANDA ANDA078643 Medsource Pharmaceuticals CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (45865-244-14)
45865-244-20 45865-244 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230710 N/A ANDA ANDA078643 Medsource Pharmaceuticals CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (45865-244-20)
45865-244-30 45865-244 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230523 N/A ANDA ANDA078643 Medsource Pharmaceuticals CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (45865-244-30)
45865-244-60 45865-244 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230223 N/A ANDA ANDA078643 Medsource Pharmaceuticals CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (45865-244-60)
45865-244-90 45865-244 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230223 N/A ANDA ANDA078643 Medsource Pharmaceuticals CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (45865-244-90)
76420-599-02 76420-599 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230902 N/A ANDA ANDA078643 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 2 TABLET, FILM COATED in 1 BOTTLE (76420-599-02)
76420-599-05 76420-599 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230902 N/A ANDA ANDA078643 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (76420-599-05)
76420-599-07 76420-599 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230902 N/A ANDA ANDA078643 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (76420-599-07)
76420-599-10 76420-599 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230902 N/A ANDA ANDA078643 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-599-10)
76420-599-14 76420-599 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230902 N/A ANDA ANDA078643 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (76420-599-14)
76420-599-20 76420-599 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230902 N/A ANDA ANDA078643 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (76420-599-20)
76420-599-30 76420-599 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230902 N/A ANDA ANDA078643 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-599-30)
76420-599-60 76420-599 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230902 N/A ANDA ANDA078643 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-599-60)
76420-599-90 76420-599 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230902 N/A ANDA ANDA078643 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-599-90)
0904-7400-04 0904-7400 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20240221 20270131 ANDA ANDA078643 Major Pharmaceuticals CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 BLISTER PACK in 1 CARTON (0904-7400-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-7400-06 0904-7400 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20240221 20270131 ANDA ANDA078643 Major Pharmaceuticals CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 50 BLISTER PACK in 1 CARTON (0904-7400-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-7401-61 0904-7401 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20240221 N/A ANDA ANDA078643 Major Pharmaceuticals CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 100 BLISTER PACK in 1 CARTON (0904-7401-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
70518-3474-2 70518-3474 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220813 N/A ANDA ANDA078643 REMEDYREPACK INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-2)
70518-3474-3 70518-3474 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220817 N/A ANDA ANDA078643 REMEDYREPACK INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-3)
70518-3474-4 70518-3474 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220823 N/A ANDA ANDA078643 REMEDYREPACK INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3474-4)
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