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
70095-017-01	70095-017	HUMAN PRESCRIPTION DRUG	Theophylline	Theophylline	TABLET, EXTENDED RELEASE	ORAL	20240322	N/A	ANDA	ANDA214806	Sun Pharmaceutical Industries Limited	THEOPHYLLINE ANHYDROUS	300 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70095-017-01)
70095-018-01	70095-018	HUMAN PRESCRIPTION DRUG	Theophylline	Theophylline	TABLET, EXTENDED RELEASE	ORAL	20240322	N/A	ANDA	ANDA214806	Sun Pharmaceutical Industries Limited	THEOPHYLLINE ANHYDROUS	450 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70095-018-01)
82638-106-02	82638-106	HUMAN PRESCRIPTION DRUG	Theophylline	Theophylline	TABLET, EXTENDED RELEASE	ORAL	20240730	N/A	ANDA	ANDA214806	Harman Finochem Limited	THEOPHYLLINE ANHYDROUS	450 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (82638-106-02)
82638-105-02	82638-105	HUMAN PRESCRIPTION DRUG	Theophylline	Theophylline	TABLET, EXTENDED RELEASE	ORAL	20240730	N/A	ANDA	ANDA214806	Harman Finochem Limited	THEOPHYLLINE ANHYDROUS	300 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (82638-105-02)