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=ANDA085472"
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
42806-562-01 42806-562 HUMAN PRESCRIPTION DRUG CHLORDIAZEPOXIDE HYDROCHLORIDE CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE, GELATIN COATED ORAL 20210511 N/A ANDA ANDA085472 Epic Pharma LLC CHLORDIAZEPOXIDE HYDROCHLORIDE 10 mg/1 100 CAPSULE, GELATIN COATED in 1 BOTTLE (42806-562-01)
42806-565-01 42806-565 HUMAN PRESCRIPTION DRUG CHLORDIAZEPOXIDE HYDROCHLORIDE CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE, GELATIN COATED ORAL 20210813 N/A ANDA ANDA085472 Epic Pharma, LLC CHLORDIAZEPOXIDE HYDROCHLORIDE 10 mg/1 100 CAPSULE, GELATIN COATED in 1 BOTTLE (42806-565-01)
43353-969-53 43353-969 HUMAN PRESCRIPTION DRUG Chlordiazepoxide Hydrochloride Chlordiazepoxide Hydrochloride CAPSULE, GELATIN COATED ORAL 20141004 N/A ANDA ANDA085472 Aphena Pharma Solutions - Tennessee, LLC CHLORDIAZEPOXIDE HYDROCHLORIDE 10 mg/1 60 CAPSULE, GELATIN COATED in 1 BOTTLE (43353-969-53)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase