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
71335-1214-6	71335-1214	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20240809	N/A	ANDA	ANDA210497	Bryant Ranch Prepack	BUPROPION HYDROCHLORIDE	300 mg/1	180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-6)
80425-0300-1	80425-0300	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230406	N/A	ANDA	ANDA210497	Advanced Rx Pharmacy of Tennessee, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0300-1)
80425-0300-2	80425-0300	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230406	N/A	ANDA	ANDA210497	Advanced Rx Pharmacy of Tennessee, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0300-2)
80425-0300-3	80425-0300	HUMAN PRESCRIPTION DRUG	Bupropion hydrochloride	Bupropion hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230406	N/A	ANDA	ANDA210497	Advanced Rx Pharmacy of Tennessee, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0300-3)
80425-0461-1	80425-0461	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20241218	N/A	ANDA	ANDA210497	Advanced Rx of Tennessee, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0461-1)
80425-0461-2	80425-0461	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20241218	N/A	ANDA	ANDA210497	Advanced Rx of Tennessee, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0461-2)
80425-0461-3	80425-0461	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20241218	N/A	ANDA	ANDA210497	Advanced Rx of Tennessee, LLC	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0461-3)
70518-2458-0	70518-2458	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20191129	N/A	ANDA	ANDA210497	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2458-0)
70518-2458-6	70518-2458	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20240812	N/A	ANDA	ANDA210497	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2458-6)
71205-465-30	71205-465	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200729	N/A	ANDA	ANDA210497	Proficient Rx LP	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-465-30)
71205-465-60	71205-465	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200729	N/A	ANDA	ANDA210497	Proficient Rx LP	BUPROPION HYDROCHLORIDE	300 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-465-60)
71205-465-90	71205-465	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200729	N/A	ANDA	ANDA210497	Proficient Rx LP	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-465-90)
71205-504-30	71205-504	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20201113	N/A	ANDA	ANDA210497	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-30)
71205-504-60	71205-504	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20201113	N/A	ANDA	ANDA210497	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-60)
71205-504-90	71205-504	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20201113	N/A	ANDA	ANDA210497	Proficient Rx LP	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-90)
70518-2772-2	70518-2772	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20220226	N/A	ANDA	ANDA210497	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2772-2)
70518-2772-4	70518-2772	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20230125	N/A	ANDA	ANDA210497	REMEDYREPACK INC.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2772-4)