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=ANDA091591"
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
71335-2264-1 71335-2264 HUMAN PRESCRIPTION DRUG Cevimeline Hydrochloride Cevimeline Hydrochloride CAPSULE ORAL 20231027 N/A ANDA ANDA091591 Bryant Ranch Prepack CEVIMELINE HYDROCHLORIDE 30 mg/1 30 CAPSULE in 1 BOTTLE (71335-2264-1)
71335-2264-2 71335-2264 HUMAN PRESCRIPTION DRUG Cevimeline Hydrochloride Cevimeline Hydrochloride CAPSULE ORAL 20231027 N/A ANDA ANDA091591 Bryant Ranch Prepack CEVIMELINE HYDROCHLORIDE 30 mg/1 60 CAPSULE in 1 BOTTLE (71335-2264-2)
71335-2264-3 71335-2264 HUMAN PRESCRIPTION DRUG Cevimeline Hydrochloride Cevimeline Hydrochloride CAPSULE ORAL 20231027 N/A ANDA ANDA091591 Bryant Ranch Prepack CEVIMELINE HYDROCHLORIDE 30 mg/1 90 CAPSULE in 1 BOTTLE (71335-2264-3)
0054-0334-25 0054-0334 HUMAN PRESCRIPTION DRUG Cevimeline Hydrochloride Cevimeline Hydrochloride CAPSULE ORAL 20130708 N/A ANDA ANDA091591 Hikma Pharmaceuticals USA Inc. CEVIMELINE HYDROCHLORIDE 30 mg/1 100 CAPSULE in 1 BOTTLE (0054-0334-25)
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