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=ANDA211623"
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
60687-594-21 60687-594 HUMAN PRESCRIPTION DRUG CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE ORAL 20211223 N/A ANDA ANDA211623 American Health Packaging CARBAMAZEPINE 400 mg/1 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-594-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-594-11)
16571-681-01 16571-681 HUMAN PRESCRIPTION DRUG CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE ORAL 20200424 N/A ANDA ANDA211623 Rising Pharma Holdings, Inc. CARBAMAZEPINE 200 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-681-01)
16571-680-01 16571-680 HUMAN PRESCRIPTION DRUG CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE ORAL 20200424 N/A ANDA ANDA211623 Rising Pharma Holdings, Inc. CARBAMAZEPINE 100 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-680-01)
16571-682-01 16571-682 HUMAN PRESCRIPTION DRUG CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE ORAL 20200424 N/A ANDA ANDA211623 Rising Pharma Holdings, Inc. CARBAMAZEPINE 400 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-682-01)
60687-583-21 60687-583 HUMAN PRESCRIPTION DRUG CARBAMAZEPINE CARBAMAZEPINE TABLET, EXTENDED RELEASE ORAL 20220105 N/A ANDA ANDA211623 American Health Packaging CARBAMAZEPINE 200 mg/1 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-583-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-583-11)
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