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
64679-102-01	64679-102	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20121121	N/A	ANDA	ANDA202189	Wockhardt USA LLC.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-102-01)
64679-102-02	64679-102	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20121121	N/A	ANDA	ANDA202189	Wockhardt USA LLC.	BUPROPION HYDROCHLORIDE	150 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-102-02)
64679-102-05	64679-102	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20121121	N/A	ANDA	ANDA202189	Wockhardt USA LLC.	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-102-05)
64679-103-01	64679-103	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220128	N/A	ANDA	ANDA202189	Wockhardt USA LLC.	BUPROPION HYDROCHLORIDE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-103-01)
64679-103-02	64679-103	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220128	N/A	ANDA	ANDA202189	Wockhardt USA LLC.	BUPROPION HYDROCHLORIDE	300 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-103-02)
64679-103-05	64679-103	HUMAN PRESCRIPTION DRUG	Bupropion Hydrochloride (XL)	Bupropion Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220128	N/A	ANDA	ANDA202189	Wockhardt USA LLC.	BUPROPION HYDROCHLORIDE	300 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-103-05)