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
80425-0200-2	80425-0200	HUMAN PRESCRIPTION DRUG	Sertraline Hydrochloride	Sertraline Hydrochloride	TABLET, FILM COATED	ORAL	20230424	N/A	ANDA	ANDA077206	Advanced Rx Pharmacy of Tennessee, LLC	SERTRALINE HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0200-2)
80425-0200-3	80425-0200	HUMAN PRESCRIPTION DRUG	Sertraline Hydrochloride	Sertraline Hydrochloride	TABLET, FILM COATED	ORAL	20230424	N/A	ANDA	ANDA077206	Advanced Rx Pharmacy of Tennessee, LLC	SERTRALINE HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0200-3)
84386-099-60	84386-099	HUMAN PRESCRIPTION DRUG	Sertraline Hydrochloride	Sertraline Hydrochloride	TABLET, FILM COATED	ORAL	20251120	N/A	ANDA	ANDA077206	Aurobindo Pharma Limited	SERTRALINE HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (84386-099-60)
84386-099-90	84386-099	HUMAN PRESCRIPTION DRUG	Sertraline Hydrochloride	Sertraline Hydrochloride	TABLET, FILM COATED	ORAL	20251120	N/A	ANDA	ANDA077206	Aurobindo Pharma Limited	SERTRALINE HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (84386-099-90)
84386-099-99	84386-099	HUMAN PRESCRIPTION DRUG	Sertraline Hydrochloride	Sertraline Hydrochloride	TABLET, FILM COATED	ORAL	20251120	N/A	ANDA	ANDA077206	Aurobindo Pharma Limited	SERTRALINE HYDROCHLORIDE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (84386-099-99)
68788-6835-9	68788-6835	HUMAN PRESCRIPTION DRUG	Sertraline Hydrochloride	Sertraline Hydrochloride	TABLET, FILM COATED	ORAL	20161121	N/A	ANDA	ANDA077206	Preferred Pharmaceuticals Inc.	SERTRALINE HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-6835-9)
84386-097-01	84386-097	HUMAN PRESCRIPTION DRUG	Sertraline Hydrochloride	Sertraline Hydrochloride	TABLET, FILM COATED	ORAL	20251120	N/A	ANDA	ANDA077206	Aurobindo Pharma Limited	SERTRALINE HYDROCHLORIDE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (84386-097-01)
84386-097-05	84386-097	HUMAN PRESCRIPTION DRUG	Sertraline Hydrochloride	Sertraline Hydrochloride	TABLET, FILM COATED	ORAL	20251120	N/A	ANDA	ANDA077206	Aurobindo Pharma Limited	SERTRALINE HYDROCHLORIDE	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (84386-097-05)
84386-097-30	84386-097	HUMAN PRESCRIPTION DRUG	Sertraline Hydrochloride	Sertraline Hydrochloride	TABLET, FILM COATED	ORAL	20251120	N/A	ANDA	ANDA077206	Aurobindo Pharma Limited	SERTRALINE HYDROCHLORIDE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (84386-097-30)
84386-097-50	84386-097	HUMAN PRESCRIPTION DRUG	Sertraline Hydrochloride	Sertraline Hydrochloride	TABLET, FILM COATED	ORAL	20251120	N/A	ANDA	ANDA077206	Aurobindo Pharma Limited	SERTRALINE HYDROCHLORIDE	25 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (84386-097-50)
84386-097-51	84386-097	HUMAN PRESCRIPTION DRUG	Sertraline Hydrochloride	Sertraline Hydrochloride	TABLET, FILM COATED	ORAL	20251120	N/A	ANDA	ANDA077206	Aurobindo Pharma Limited	SERTRALINE HYDROCHLORIDE	25 mg/1	5000 TABLET, FILM COATED in 1 BOTTLE (84386-097-51)
84386-097-60	84386-097	HUMAN PRESCRIPTION DRUG	Sertraline Hydrochloride	Sertraline Hydrochloride	TABLET, FILM COATED	ORAL	20251120	N/A	ANDA	ANDA077206	Aurobindo Pharma Limited	SERTRALINE HYDROCHLORIDE	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (84386-097-60)
84386-097-90	84386-097	HUMAN PRESCRIPTION DRUG	Sertraline Hydrochloride	Sertraline Hydrochloride	TABLET, FILM COATED	ORAL	20251120	N/A	ANDA	ANDA077206	Aurobindo Pharma Limited	SERTRALINE HYDROCHLORIDE	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (84386-097-90)
84386-097-99	84386-097	HUMAN PRESCRIPTION DRUG	Sertraline Hydrochloride	Sertraline Hydrochloride	TABLET, FILM COATED	ORAL	20251120	N/A	ANDA	ANDA077206	Aurobindo Pharma Limited	SERTRALINE HYDROCHLORIDE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (84386-097-99)