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=ANDA091281"
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
55700-858-60 55700-858 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20200417 N/A ANDA ANDA091281 Quality Care Products, LLC CYCLOBENZAPRINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55700-858-60)
71205-857-11 71205-857 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20220506 N/A ANDA ANDA091281 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 15 mg/1 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-857-11)
71205-857-00 71205-857 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20220506 N/A ANDA ANDA091281 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 15 mg/1 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-857-00)
71205-857-55 71205-857 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20220506 N/A ANDA ANDA091281 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 15 mg/1 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-857-55)
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