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=ANDA090100"
符合检索条件的记录共 12 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
65841-749-01 65841-749 HUMAN PRESCRIPTION DRUG donepezil hydrochloride donepezil hydrochloride TABLET, FILM COATED ORAL 20110525 N/A ANDA ANDA090100 Zydus Lifesciences Limited DONEPEZIL HYDROCHLORIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-749-01)
65841-749-05 65841-749 HUMAN PRESCRIPTION DRUG donepezil hydrochloride donepezil hydrochloride TABLET, FILM COATED ORAL 20110525 N/A ANDA ANDA090100 Zydus Lifesciences Limited DONEPEZIL HYDROCHLORIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-749-05)
65841-749-06 65841-749 HUMAN PRESCRIPTION DRUG donepezil hydrochloride donepezil hydrochloride TABLET, FILM COATED ORAL 20110525 N/A ANDA ANDA090100 Zydus Lifesciences Limited DONEPEZIL HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65841-749-06)
65841-749-10 65841-749 HUMAN PRESCRIPTION DRUG donepezil hydrochloride donepezil hydrochloride TABLET, FILM COATED ORAL 20110525 N/A ANDA ANDA090100 Zydus Lifesciences Limited DONEPEZIL HYDROCHLORIDE 5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65841-749-10)
65841-749-16 65841-749 HUMAN PRESCRIPTION DRUG donepezil hydrochloride donepezil hydrochloride TABLET, FILM COATED ORAL 20110525 N/A ANDA ANDA090100 Zydus Lifesciences Limited DONEPEZIL HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65841-749-16)
65841-749-30 65841-749 HUMAN PRESCRIPTION DRUG donepezil hydrochloride donepezil hydrochloride TABLET, FILM COATED ORAL 20110525 N/A ANDA ANDA090100 Zydus Lifesciences Limited DONEPEZIL HYDROCHLORIDE 5 mg/1 10 BLISTER PACK in 1 CARTON (65841-749-30) / 10 TABLET, FILM COATED in 1 BLISTER PACK
65841-750-01 65841-750 HUMAN PRESCRIPTION DRUG donepezil hydrochloride donepezil hydrochloride TABLET, FILM COATED ORAL 20110525 N/A ANDA ANDA090100 Zydus Lifesciences Limited DONEPEZIL HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-750-01)
65841-750-05 65841-750 HUMAN PRESCRIPTION DRUG donepezil hydrochloride donepezil hydrochloride TABLET, FILM COATED ORAL 20110525 N/A ANDA ANDA090100 Zydus Lifesciences Limited DONEPEZIL HYDROCHLORIDE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-750-05)
65841-750-06 65841-750 HUMAN PRESCRIPTION DRUG donepezil hydrochloride donepezil hydrochloride TABLET, FILM COATED ORAL 20110525 N/A ANDA ANDA090100 Zydus Lifesciences Limited DONEPEZIL HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65841-750-06)
65841-750-10 65841-750 HUMAN PRESCRIPTION DRUG donepezil hydrochloride donepezil hydrochloride TABLET, FILM COATED ORAL 20110525 N/A ANDA ANDA090100 Zydus Lifesciences Limited DONEPEZIL HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65841-750-10)
65841-750-16 65841-750 HUMAN PRESCRIPTION DRUG donepezil hydrochloride donepezil hydrochloride TABLET, FILM COATED ORAL 20110525 N/A ANDA ANDA090100 Zydus Lifesciences Limited DONEPEZIL HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65841-750-16)
65841-750-30 65841-750 HUMAN PRESCRIPTION DRUG donepezil hydrochloride donepezil hydrochloride TABLET, FILM COATED ORAL 20110525 N/A ANDA ANDA090100 Zydus Lifesciences Limited DONEPEZIL HYDROCHLORIDE 10 mg/1 10 BLISTER PACK in 1 CARTON (65841-750-30) / 10 TABLET, FILM COATED in 1 BLISTER PACK
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