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=ANDA218613"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
71921-250-36 71921-250 HUMAN PRESCRIPTION DRUG Lofexidine Lofexidine TABLET, COATED ORAL 20240821 N/A ANDA ANDA218613 Florida Pharmaceutical Products, LLC LOFEXIDINE HYDROCHLORIDE .18 mg/1 1 BOTTLE in 1 CARTON (71921-250-36) / 36 TABLET, COATED in 1 BOTTLE
71921-250-96 71921-250 HUMAN PRESCRIPTION DRUG Lofexidine Lofexidine TABLET, COATED ORAL 20240821 N/A ANDA ANDA218613 Florida Pharmaceutical Products, LLC LOFEXIDINE HYDROCHLORIDE .18 mg/1 1 BOTTLE in 1 CARTON (71921-250-96) / 96 TABLET, COATED in 1 BOTTLE
14445-146-36 14445-146 HUMAN PRESCRIPTION DRUG Lofexidine Lofexidine TABLET, COATED ORAL 20240821 N/A ANDA ANDA218613 Indoco Remedies Limited LOFEXIDINE HYDROCHLORIDE .18 mg/1 1 BOTTLE in 1 CARTON (14445-146-36) / 36 TABLET, COATED in 1 BOTTLE
14445-146-96 14445-146 HUMAN PRESCRIPTION DRUG Lofexidine Lofexidine TABLET, COATED ORAL 20240821 N/A ANDA ANDA218613 Indoco Remedies Limited LOFEXIDINE HYDROCHLORIDE .18 mg/1 1 BOTTLE in 1 CARTON (14445-146-96) / 96 TABLET, COATED in 1 BOTTLE
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