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
72578-174-01	72578-174	HUMAN PRESCRIPTION DRUG	Theophylline	Theophylline	TABLET, EXTENDED RELEASE	ORAL	20240525	N/A	ANDA	ANDA218063	Viona Pharmaceuticals Inc	THEOPHYLLINE ANHYDROUS	450 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72578-174-01)
72578-173-01	72578-173	HUMAN PRESCRIPTION DRUG	Theophylline	Theophylline	TABLET, EXTENDED RELEASE	ORAL	20240525	N/A	ANDA	ANDA218063	Viona Pharmaceuticals Inc	THEOPHYLLINE ANHYDROUS	300 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72578-173-01)
70771-1783-1	70771-1783	HUMAN PRESCRIPTION DRUG	Theophylline	Theophylline	TABLET, EXTENDED RELEASE	ORAL	20240525	N/A	ANDA	ANDA218063	Zydus Lifesciences Limited	THEOPHYLLINE ANHYDROUS	450 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1783-1)
70771-1782-1	70771-1782	HUMAN PRESCRIPTION DRUG	Theophylline	Theophylline	TABLET, EXTENDED RELEASE	ORAL	20240525	N/A	ANDA	ANDA218063	Zydus Lifesciences Limited	THEOPHYLLINE ANHYDROUS	300 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1782-1)