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
43063-744-30	43063-744	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE SR	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20170209	N/A	ANDA	ANDA206674	PD-Rx Pharmaceuticals, Inc.	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-744-30)
69097-877-07	69097-877	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160725	N/A	ANDA	ANDA206674	Cipla USA Inc.,	BUPROPION HYDROCHLORIDE	100 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-877-07)
69097-878-02	69097-878	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160725	N/A	ANDA	ANDA206674	Cipla USA Inc.,	BUPROPION HYDROCHLORIDE	150 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-878-02)
69097-878-03	69097-878	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160725	N/A	ANDA	ANDA206674	Cipla USA Inc.,	BUPROPION HYDROCHLORIDE	150 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-878-03)
69097-878-07	69097-878	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160725	N/A	ANDA	ANDA206674	Cipla USA Inc.,	BUPROPION HYDROCHLORIDE	150 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-878-07)
69097-878-12	69097-878	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160725	N/A	ANDA	ANDA206674	Cipla USA Inc.,	BUPROPION HYDROCHLORIDE	150 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-878-12)
69097-879-02	69097-879	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160725	N/A	ANDA	ANDA206674	Cipla USA Inc.,	BUPROPION HYDROCHLORIDE	200 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-879-02)
69097-879-03	69097-879	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160725	N/A	ANDA	ANDA206674	Cipla USA Inc.,	BUPROPION HYDROCHLORIDE	200 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-879-03)
69097-879-07	69097-879	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160725	N/A	ANDA	ANDA206674	Cipla USA Inc.,	BUPROPION HYDROCHLORIDE	200 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-879-07)
69097-879-12	69097-879	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160725	N/A	ANDA	ANDA206674	Cipla USA Inc.,	BUPROPION HYDROCHLORIDE	200 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-879-12)
69097-877-03	69097-877	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160725	N/A	ANDA	ANDA206674	Cipla USA Inc.,	BUPROPION HYDROCHLORIDE	100 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-877-03)
69097-877-02	69097-877	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160725	N/A	ANDA	ANDA206674	Cipla USA Inc.,	BUPROPION HYDROCHLORIDE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-877-02)
69097-877-12	69097-877	HUMAN PRESCRIPTION DRUG	BUPROPION HYDROCHLORIDE (SR)	Bupropion Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20160725	N/A	ANDA	ANDA206674	Cipla USA Inc.,	BUPROPION HYDROCHLORIDE	100 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-877-12)