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
53489-148-01	53489-148	HUMAN PRESCRIPTION DRUG	Thioridazine Hydrochloride	Thioridazine Hydrochloride	TABLET, FILM COATED	ORAL	19881007	N/A	ANDA	ANDA089953	Sun Pharmaceutical Industries, Inc.	THIORIDAZINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-148-01)
53489-148-10	53489-148	HUMAN PRESCRIPTION DRUG	Thioridazine Hydrochloride	Thioridazine Hydrochloride	TABLET, FILM COATED	ORAL	19881007	N/A	ANDA	ANDA089953	Sun Pharmaceutical Industries, Inc.	THIORIDAZINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-148-10)
53489-149-01	53489-149	HUMAN PRESCRIPTION DRUG	Thioridazine Hydrochloride	Thioridazine Hydrochloride	TABLET, FILM COATED	ORAL	19881007	N/A	ANDA	ANDA089953	Sun Pharmaceutical Industries, Inc.	THIORIDAZINE HYDROCHLORIDE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-149-01)
53489-149-10	53489-149	HUMAN PRESCRIPTION DRUG	Thioridazine Hydrochloride	Thioridazine Hydrochloride	TABLET, FILM COATED	ORAL	19881007	N/A	ANDA	ANDA089953	Sun Pharmaceutical Industries, Inc.	THIORIDAZINE HYDROCHLORIDE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-149-10)
53489-150-01	53489-150	HUMAN PRESCRIPTION DRUG	Thioridazine Hydrochloride	Thioridazine Hydrochloride	TABLET, FILM COATED	ORAL	19881007	N/A	ANDA	ANDA089953	Sun Pharmaceutical Industries, Inc.	THIORIDAZINE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-150-01)
53489-150-10	53489-150	HUMAN PRESCRIPTION DRUG	Thioridazine Hydrochloride	Thioridazine Hydrochloride	TABLET, FILM COATED	ORAL	19881007	N/A	ANDA	ANDA089953	Sun Pharmaceutical Industries, Inc.	THIORIDAZINE HYDROCHLORIDE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-150-10)
53489-500-01	53489-500	HUMAN PRESCRIPTION DRUG	Thioridazine Hydrochloride	Thioridazine Hydrochloride	TABLET, FILM COATED	ORAL	19881007	N/A	ANDA	ANDA089953	Sun Pharmaceutical Industries, Inc.	THIORIDAZINE HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-01)
53489-500-02	53489-500	HUMAN PRESCRIPTION DRUG	Thioridazine Hydrochloride	Thioridazine Hydrochloride	TABLET, FILM COATED	ORAL	19881007	N/A	ANDA	ANDA089953	Sun Pharmaceutical Industries, Inc.	THIORIDAZINE HYDROCHLORIDE	100 mg/1	50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-02)
53489-500-03	53489-500	HUMAN PRESCRIPTION DRUG	Thioridazine Hydrochloride	Thioridazine Hydrochloride	TABLET, FILM COATED	ORAL	19881007	N/A	ANDA	ANDA089953	Sun Pharmaceutical Industries, Inc.	THIORIDAZINE HYDROCHLORIDE	100 mg/1	250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-03)
53489-500-05	53489-500	HUMAN PRESCRIPTION DRUG	Thioridazine Hydrochloride	Thioridazine Hydrochloride	TABLET, FILM COATED	ORAL	19881007	N/A	ANDA	ANDA089953	Sun Pharmaceutical Industries, Inc.	THIORIDAZINE HYDROCHLORIDE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-05)
53489-500-06	53489-500	HUMAN PRESCRIPTION DRUG	Thioridazine Hydrochloride	Thioridazine Hydrochloride	TABLET, FILM COATED	ORAL	19881007	N/A	ANDA	ANDA089953	Sun Pharmaceutical Industries, Inc.	THIORIDAZINE HYDROCHLORIDE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-06)
53489-500-10	53489-500	HUMAN PRESCRIPTION DRUG	Thioridazine Hydrochloride	Thioridazine Hydrochloride	TABLET, FILM COATED	ORAL	19881007	N/A	ANDA	ANDA089953	Sun Pharmaceutical Industries, Inc.	THIORIDAZINE HYDROCHLORIDE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-10)
53489-500-60	53489-500	HUMAN PRESCRIPTION DRUG	Thioridazine Hydrochloride	Thioridazine Hydrochloride	TABLET, FILM COATED	ORAL	19881007	N/A	ANDA	ANDA089953	Sun Pharmaceutical Industries, Inc.	THIORIDAZINE HYDROCHLORIDE	100 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-60)