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）

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
35561-357-12	35561-357	HUMAN PRESCRIPTION DRUG	CARBAMAZEPINE ER	carbamazepine	TABLET, EXTENDED RELEASE	ORAL	20211209	N/A	ANDA	ANDA215591	AustarPharma LLC	CARBAMAZEPINE	400 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (35561-357-12)
35561-356-12	35561-356	HUMAN PRESCRIPTION DRUG	CARBAMAZEPINE ER	carbamazepine	TABLET, EXTENDED RELEASE	ORAL	20211209	N/A	ANDA	ANDA215591	AustarPharma LLC	CARBAMAZEPINE	200 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (35561-356-12)
35561-355-12	35561-355	HUMAN PRESCRIPTION DRUG	CARBAMAZEPINE ER	carbamazepine	TABLET, EXTENDED RELEASE	ORAL	20211209	N/A	ANDA	ANDA215591	AustarPharma LLC	CARBAMAZEPINE	100 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (35561-355-12)
62135-927-60	62135-927	HUMAN PRESCRIPTION DRUG	Carbamazepine ER	Carbamazepine ER	TABLET, EXTENDED RELEASE	ORAL	20241106	N/A	ANDA	ANDA215591	Chartwell RX, LLC	CARBAMAZEPINE	100 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (62135-927-60)
62135-928-60	62135-928	HUMAN PRESCRIPTION DRUG	Carbamazepine ER	Carbamazepine ER	TABLET, EXTENDED RELEASE	ORAL	20241106	N/A	ANDA	ANDA215591	Chartwell RX, LLC	CARBAMAZEPINE	200 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (62135-928-60)
62135-930-60	62135-930	HUMAN PRESCRIPTION DRUG	Carbamazepine ER	Carbamazepine ER	TABLET, EXTENDED RELEASE	ORAL	20241106	N/A	ANDA	ANDA215591	Chartwell RX, LLC	CARBAMAZEPINE	400 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (62135-930-60)