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=ANDA090175"
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
65841-722-30 65841-722 HUMAN PRESCRIPTION DRUG donepezil hydrochloride donepezil hydrochloride TABLET, ORALLY DISINTEGRATING ORAL 20110511 N/A ANDA ANDA090175 Zydus Lifesciences Limited DONEPEZIL HYDROCHLORIDE 10 mg/1 10 BLISTER PACK in 1 CARTON (65841-722-30) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
65841-722-06 65841-722 HUMAN PRESCRIPTION DRUG donepezil hydrochloride donepezil hydrochloride TABLET, ORALLY DISINTEGRATING ORAL 20110511 N/A ANDA ANDA090175 Zydus Lifesciences Limited DONEPEZIL HYDROCHLORIDE 10 mg/1 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65841-722-06)
65841-722-10 65841-722 HUMAN PRESCRIPTION DRUG donepezil hydrochloride donepezil hydrochloride TABLET, ORALLY DISINTEGRATING ORAL 20110511 N/A ANDA ANDA090175 Zydus Lifesciences Limited DONEPEZIL HYDROCHLORIDE 10 mg/1 1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65841-722-10)
65841-722-16 65841-722 HUMAN PRESCRIPTION DRUG donepezil hydrochloride donepezil hydrochloride TABLET, ORALLY DISINTEGRATING ORAL 20110511 N/A ANDA ANDA090175 Zydus Lifesciences Limited DONEPEZIL HYDROCHLORIDE 10 mg/1 90 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (65841-722-16)
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