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=ANDA090478"
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
76282-283-10 76282-283 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET ORAL 20250410 N/A ANDA ANDA090478 EXELAN PHARMACEUTICALS, INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 1000 TABLET in 1 BOTTLE (76282-283-10)
76282-283-18 76282-283 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET ORAL 20250410 N/A ANDA ANDA090478 EXELAN PHARMACEUTICALS, INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 180 TABLET in 1 BOTTLE (76282-283-18)
50268-190-15 50268-190 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20140610 N/A ANDA ANDA090478 AvPAK CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 50 BLISTER PACK in 1 BOX (50268-190-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-190-11)
50268-191-15 50268-191 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20220801 N/A ANDA ANDA090478 AvPAK CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 50 BLISTER PACK in 1 BOX (50268-191-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-191-11)
60687-558-01 60687-558 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20220210 N/A ANDA ANDA090478 American Health Packaging CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 100 BLISTER PACK in 1 CARTON (60687-558-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-558-11)
0615-8084-05 0615-8084 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20160722 N/A ANDA ANDA090478 NCS HealthCare of KY, LLC dba Vangard Labs CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8084-05)
0615-8084-39 0615-8084 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20160722 N/A ANDA ANDA090478 NCS HealthCare of KY, LLC dba Vangard Labs CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8084-39)
51655-973-20 51655-973 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20221017 N/A ANDA ANDA090478 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-20)
51655-973-25 51655-973 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20220906 N/A ANDA ANDA090478 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-25)
51655-973-52 51655-973 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20221007 N/A ANDA ANDA090478 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-52)
51655-973-53 51655-973 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20220727 N/A ANDA ANDA090478 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-53)
51655-973-54 51655-973 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20220824 N/A ANDA ANDA090478 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-54)
51655-973-87 51655-973 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20220504 N/A ANDA ANDA090478 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-87)
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