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
72241-030-22	72241-030	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20211020	N/A	ANDA	ANDA212645	Modavar Pharmaceuticals LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72241-030-22)
72241-031-10	72241-031	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20211020	N/A	ANDA	ANDA212645	Modavar Pharmaceuticals LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	37.5 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72241-031-10)
72241-031-22	72241-031	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20211020	N/A	ANDA	ANDA212645	Modavar Pharmaceuticals LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	37.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72241-031-22)
72241-030-10	72241-030	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20211020	N/A	ANDA	ANDA212645	Modavar Pharmaceuticals LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	25 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72241-030-10)
72241-029-22	72241-029	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20211020	N/A	ANDA	ANDA212645	Modavar Pharmaceuticals LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	12.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72241-029-22)
72241-029-10	72241-029	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20211020	N/A	ANDA	ANDA212645	Modavar Pharmaceuticals LLC	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	12.5 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72241-029-10)
71209-094-01	71209-094	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200214	N/A	ANDA	ANDA212645	Cadila Pharmaceuticals Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	12.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71209-094-01)
71209-094-10	71209-094	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200214	N/A	ANDA	ANDA212645	Cadila Pharmaceuticals Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	12.5 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71209-094-10)
71209-096-01	71209-096	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200214	N/A	ANDA	ANDA212645	Cadila Pharmaceuticals Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	37.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71209-096-01)
71209-096-10	71209-096	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200214	N/A	ANDA	ANDA212645	Cadila Pharmaceuticals Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	37.5 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71209-096-10)
71209-095-01	71209-095	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200214	N/A	ANDA	ANDA212645	Cadila Pharmaceuticals Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	25 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71209-095-01)
71209-095-10	71209-095	HUMAN PRESCRIPTION DRUG	Paroxetine	Paroxetine	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200214	N/A	ANDA	ANDA212645	Cadila Pharmaceuticals Limited	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	25 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71209-095-10)