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
0049-4900-41	0049-4900	HUMAN PRESCRIPTION DRUG	Zoloft	sertraline hydrochloride	TABLET, FILM COATED	ORAL	19920211	N/A	NDA	NDA019839	ROERIG	SERTRALINE HYDROCHLORIDE	50 mg/1	100 BLISTER PACK in 1 CARTON (0049-4900-41) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0049-4910-30	0049-4910	HUMAN PRESCRIPTION DRUG	Zoloft	sertraline hydrochloride	TABLET, FILM COATED	ORAL	19920211	N/A	NDA	NDA019839	ROERIG	SERTRALINE HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0049-4910-30)
0049-4910-41	0049-4910	HUMAN PRESCRIPTION DRUG	Zoloft	sertraline hydrochloride	TABLET, FILM COATED	ORAL	19920211	N/A	NDA	NDA019839	ROERIG	SERTRALINE HYDROCHLORIDE	100 mg/1	100 BLISTER PACK in 1 CARTON (0049-4910-41) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0049-4960-30	0049-4960	HUMAN PRESCRIPTION DRUG	Zoloft	sertraline hydrochloride	TABLET, FILM COATED	ORAL	19920211	20251031	NDA	NDA019839	ROERIG	SERTRALINE HYDROCHLORIDE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0049-4960-30)
0049-4900-30	0049-4900	HUMAN PRESCRIPTION DRUG	Zoloft	sertraline hydrochloride	TABLET, FILM COATED	ORAL	19920211	N/A	NDA	NDA019839	ROERIG	SERTRALINE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0049-4900-30)
58151-574-93	58151-574	HUMAN PRESCRIPTION DRUG	Zoloft	sertraline hydrochloride	TABLET, FILM COATED	ORAL	20241030	N/A	NDA	NDA019839	Viatris Specialty LLC	SERTRALINE HYDROCHLORIDE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (58151-574-93)
71610-433-15	71610-433	HUMAN PRESCRIPTION DRUG	SERTRALINE HYDROCHLORIDE	sertraline hydrochloride	TABLET, FILM COATED	ORAL	20200616	N/A	NDA AUTHORIZED GENERIC	NDA019839	Aphena Pharma Solutions - Tennessee, LLC	SERTRALINE HYDROCHLORIDE	100 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71610-433-15)