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=ANDA074871"
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
50090-2918-0 50090-2918 HUMAN PRESCRIPTION DRUG Selegiline Hydrochloride Selegiline Hydrochloride TABLET ORAL 20170314 N/A ANDA ANDA074871 A-S Medication Solutions SELEGILINE HYDROCHLORIDE 5 mg/1 4 TABLET in 1 BOTTLE (50090-2918-0)
60429-176-60 60429-176 HUMAN PRESCRIPTION DRUG Selegiline Hydrochloride Selegiline Hydrochloride TABLET ORAL 20130402 N/A ANDA ANDA074871 Golden State Medical Supply, Inc. SELEGILINE HYDROCHLORIDE 5 mg/1 60 TABLET in 1 BOTTLE (60429-176-60)
60505-3438-3 60505-3438 HUMAN PRESCRIPTION DRUG Selegiline Hydrochloride Selegiline Hydrochloride TABLET ORAL 19970706 N/A ANDA ANDA074871 Apotex Corp. SELEGILINE HYDROCHLORIDE 5 mg/1 60 TABLET in 1 BOTTLE (60505-3438-3)
60505-3438-8 60505-3438 HUMAN PRESCRIPTION DRUG Selegiline Hydrochloride Selegiline Hydrochloride TABLET ORAL 19970706 N/A ANDA ANDA074871 Apotex Corp. SELEGILINE HYDROCHLORIDE 5 mg/1 500 TABLET in 1 BOTTLE (60505-3438-8)
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