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=ANDA201146"
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
0615-8313-39 0615-8313 HUMAN PRESCRIPTION DRUG Donepezil Hydrochloride Donepezil Hydrochloride TABLET, FILM COATED ORAL 20190821 N/A ANDA ANDA201146 NCS HealthCare of KY, LLC dba Vangard Labs DONEPEZIL HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8313-39)
71335-2022-1 71335-2022 HUMAN PRESCRIPTION DRUG Donepezil Hydrochloride Donepezil Hydrochloride TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA201146 Bryant Ranch Prepack DONEPEZIL HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-2022-1)
71335-2022-2 71335-2022 HUMAN PRESCRIPTION DRUG Donepezil Hydrochloride Donepezil Hydrochloride TABLET, FILM COATED ORAL 20211222 N/A ANDA ANDA201146 Bryant Ranch Prepack DONEPEZIL HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2022-2)
71335-2022-3 71335-2022 HUMAN PRESCRIPTION DRUG Donepezil Hydrochloride Donepezil Hydrochloride TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA201146 Bryant Ranch Prepack DONEPEZIL HYDROCHLORIDE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-2022-3)
50090-6329-0 50090-6329 HUMAN PRESCRIPTION DRUG Donepezil Hydrochloride Donepezil Hydrochloride TABLET, FILM COATED ORAL 20230116 N/A ANDA ANDA201146 A-S Medication Solutions DONEPEZIL HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6329-0)
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