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=ANDA090048"
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
55111-596-05 55111-596 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride TABLET, FILM COATED ORAL 20150711 N/A ANDA ANDA090048 Dr. Reddys Laboratories Limited MEMANTINE HYDROCHLORIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (55111-596-05)
55111-596-30 55111-596 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride TABLET, FILM COATED ORAL 20150711 N/A ANDA ANDA090048 Dr. Reddys Laboratories Limited MEMANTINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (55111-596-30)
55111-596-60 55111-596 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride TABLET, FILM COATED ORAL 20150711 N/A ANDA ANDA090048 Dr. Reddys Laboratories Limited MEMANTINE HYDROCHLORIDE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (55111-596-60)
55111-596-78 55111-596 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride TABLET, FILM COATED ORAL 20150711 N/A ANDA ANDA090048 Dr. Reddys Laboratories Limited MEMANTINE HYDROCHLORIDE 5 mg/1 10 BLISTER PACK in 1 CARTON (55111-596-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK
55111-596-79 55111-596 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride TABLET, FILM COATED ORAL 20150711 N/A ANDA ANDA090048 Dr. Reddys Laboratories Limited MEMANTINE HYDROCHLORIDE 5 mg/1 1 BLISTER PACK in 1 CARTON (55111-596-79) / 10 TABLET, FILM COATED in 1 BLISTER PACK
55154-4151-0 55154-4151 HUMAN PRESCRIPTION DRUG Memantine Hydrochloride Memantine Hydrochloride TABLET, FILM COATED ORAL 20220512 N/A ANDA ANDA090048 Cardinal Health 107, LLC MEMANTINE HYDROCHLORIDE 5 mg/1 10 BLISTER PACK in 1 BAG (55154-4151-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase