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
31722-488-05	31722-488	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20251001	N/A	ANDA	ANDA217898	Camber Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-488-05)
31722-488-30	31722-488	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20251001	N/A	ANDA	ANDA217898	Camber Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-488-30)
31722-488-90	31722-488	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20251001	N/A	ANDA	ANDA217898	Camber Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-488-90)
31722-487-90	31722-487	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20251001	N/A	ANDA	ANDA217898	Camber Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-487-90)
31722-487-30	31722-487	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20251001	N/A	ANDA	ANDA217898	Camber Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-487-30)
31722-487-05	31722-487	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20251001	N/A	ANDA	ANDA217898	Camber Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-487-05)