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
47781-637-30	47781-637	HUMAN PRESCRIPTION DRUG	bupropion hydrochloride	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180928	20260301	NDA AUTHORIZED GENERIC	NDA022497	Alvogen Inc.	BUPROPION HYDROCHLORIDE	450 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47781-637-30)
52427-575-30	52427-575	HUMAN PRESCRIPTION DRUG	Forfivo XL	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20170515	20250101	NDA	NDA022497	Almatica Pharma Inc.	BUPROPION HYDROCHLORIDE	450 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (52427-575-30)
64679-830-01	64679-830	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180809	N/A	NDA AUTHORIZED GENERIC	NDA022497	Wockhardt USA LLC.	BUPROPION HYDROCHLORIDE	450 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-830-01)
24979-247-06	24979-247	HUMAN PRESCRIPTION DRUG	Forfivo XL	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231215	N/A	NDA	NDA022497	TWi Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	450 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-247-06)
24979-248-06	24979-248	HUMAN PRESCRIPTION DRUG	bupropion hydrochloride	bupropion hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20231215	N/A	NDA AUTHORIZED GENERIC	NDA022497	TWi Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	450 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-248-06)