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=ANDA212948"
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
71930-074-90 71930-074 HUMAN PRESCRIPTION DRUG Carbamazepine ER Carbamazepine TABLET, EXTENDED RELEASE ORAL 20211015 N/A ANDA ANDA212948 Eywa Pharma Inc CARBAMAZEPINE 400 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71930-074-90)
71930-074-12 71930-074 HUMAN PRESCRIPTION DRUG Carbamazepine ER Carbamazepine TABLET, EXTENDED RELEASE ORAL 20211015 N/A ANDA ANDA212948 Eywa Pharma Inc CARBAMAZEPINE 400 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71930-074-12)
71930-073-12 71930-073 HUMAN PRESCRIPTION DRUG Carbamazepine ER Carbamazepine TABLET, EXTENDED RELEASE ORAL 20211015 N/A ANDA ANDA212948 Eywa Pharma Inc CARBAMAZEPINE 200 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71930-073-12)
71930-072-12 71930-072 HUMAN PRESCRIPTION DRUG Carbamazepine ER Carbamazepine TABLET, EXTENDED RELEASE ORAL 20211015 N/A ANDA ANDA212948 Eywa Pharma Inc CARBAMAZEPINE 100 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71930-072-12)
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