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=ANDA203775"
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
16571-657-10 16571-657 HUMAN PRESCRIPTION DRUG Cevimeline Hydrochloride Cevimeline Hydrochloride CAPSULE ORAL 20140617 N/A ANDA ANDA203775 Rising Pharma Holdings, Inc. CEVIMELINE HYDROCHLORIDE 30 mg/1 100 CAPSULE in 1 BOTTLE (16571-657-10)
63629-9863-1 63629-9863 HUMAN PRESCRIPTION DRUG Cevimeline Hydrochloride Cevimeline Hydrochloride CAPSULE ORAL 20231027 N/A ANDA ANDA203775 Bryant Ranch Prepack CEVIMELINE HYDROCHLORIDE 30 mg/1 30 CAPSULE in 1 BOTTLE (63629-9863-1)
63629-9863-2 63629-9863 HUMAN PRESCRIPTION DRUG Cevimeline Hydrochloride Cevimeline Hydrochloride CAPSULE ORAL 20231027 N/A ANDA ANDA203775 Bryant Ranch Prepack CEVIMELINE HYDROCHLORIDE 30 mg/1 60 CAPSULE in 1 BOTTLE (63629-9863-2)
63629-9863-3 63629-9863 HUMAN PRESCRIPTION DRUG Cevimeline Hydrochloride Cevimeline Hydrochloride CAPSULE ORAL 20231027 N/A ANDA ANDA203775 Bryant Ranch Prepack CEVIMELINE HYDROCHLORIDE 30 mg/1 90 CAPSULE in 1 BOTTLE (63629-9863-3)
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