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=ANDA078518"
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
71335-1341-4 71335-1341 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20200904 N/A ANDA ANDA078518 Bryant Ranch Prepack VALACYCLOVIR HYDROCHLORIDE 500 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (71335-1341-4)
71335-1341-5 71335-1341 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20200522 N/A ANDA ANDA078518 Bryant Ranch Prepack VALACYCLOVIR HYDROCHLORIDE 500 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-1341-5)
71335-1341-6 71335-1341 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20190912 N/A ANDA ANDA078518 Bryant Ranch Prepack VALACYCLOVIR HYDROCHLORIDE 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1341-6)
71335-1341-7 71335-1341 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20200116 N/A ANDA ANDA078518 Bryant Ranch Prepack VALACYCLOVIR HYDROCHLORIDE 500 mg/1 8 TABLET, FILM COATED in 1 BOTTLE (71335-1341-7)
71335-1341-8 71335-1341 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20211228 N/A ANDA ANDA078518 Bryant Ranch Prepack VALACYCLOVIR HYDROCHLORIDE 500 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1341-8)
71335-1341-9 71335-1341 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20200204 N/A ANDA ANDA078518 Bryant Ranch Prepack VALACYCLOVIR HYDROCHLORIDE 500 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71335-1341-9)
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