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=ANDA215001"
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
71610-648-60 71610-648 HUMAN PRESCRIPTION DRUG Loperamide Hydrochloride Loperamide Hydrochloride CAPSULE ORAL 20220502 N/A ANDA ANDA215001 Aphena Pharma Solutions - Tennessee, LLC LOPERAMIDE HYDROCHLORIDE 2 mg/1 90 CAPSULE in 1 BOTTLE (71610-648-60)
60468-005-01 60468-005 HUMAN PRESCRIPTION DRUG Loperamide Hydrochloride LOPERAMIDE HYDROCHLORIDE CAPSULE ORAL 20200925 N/A ANDA ANDA215001 allphamed Pharbil Arzneimittel GmbH LOPERAMIDE HYDROCHLORIDE 2 mg/1 100 CAPSULE in 1 BOTTLE (60468-005-01)
60468-005-05 60468-005 HUMAN PRESCRIPTION DRUG Loperamide Hydrochloride LOPERAMIDE HYDROCHLORIDE CAPSULE ORAL 20200925 N/A ANDA ANDA215001 allphamed Pharbil Arzneimittel GmbH LOPERAMIDE HYDROCHLORIDE 2 mg/1 500 CAPSULE in 1 BOTTLE (60468-005-05)
60468-005-30 60468-005 HUMAN PRESCRIPTION DRUG Loperamide Hydrochloride LOPERAMIDE HYDROCHLORIDE CAPSULE ORAL 20200925 N/A ANDA ANDA215001 allphamed Pharbil Arzneimittel GmbH LOPERAMIDE HYDROCHLORIDE 2 mg/1 30 CAPSULE in 1 BOTTLE (60468-005-30)
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