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
70710-1062-1	70710-1062	HUMAN PRESCRIPTION DRUG	Albuterol	Albuterol	TABLET	ORAL	20201023	N/A	ANDA	ANDA208884	Zydus Pharmaceuticals USA Inc.	ALBUTEROL SULFATE	4 mg/1	100 TABLET in 1 BOTTLE (70710-1062-1)
70710-1062-5	70710-1062	HUMAN PRESCRIPTION DRUG	Albuterol	Albuterol	TABLET	ORAL	20201023	N/A	ANDA	ANDA208884	Zydus Pharmaceuticals USA Inc.	ALBUTEROL SULFATE	4 mg/1	500 TABLET in 1 BOTTLE (70710-1062-5)
70710-1061-1	70710-1061	HUMAN PRESCRIPTION DRUG	Albuterol	Albuterol	TABLET	ORAL	20201023	N/A	ANDA	ANDA208884	Zydus Pharmaceuticals USA Inc.	ALBUTEROL SULFATE	2 mg/1	100 TABLET in 1 BOTTLE (70710-1061-1)
70771-1512-1	70771-1512	HUMAN PRESCRIPTION DRUG	Albuterol	Albuterol	TABLET	ORAL	20201023	N/A	ANDA	ANDA208884	Zydus Lifesciences Limited	ALBUTEROL SULFATE	4 mg/1	100 TABLET in 1 BOTTLE (70771-1512-1)
70771-1512-5	70771-1512	HUMAN PRESCRIPTION DRUG	Albuterol	Albuterol	TABLET	ORAL	20201023	N/A	ANDA	ANDA208884	Zydus Lifesciences Limited	ALBUTEROL SULFATE	4 mg/1	500 TABLET in 1 BOTTLE (70771-1512-5)
70771-1511-1	70771-1511	HUMAN PRESCRIPTION DRUG	Albuterol	Albuterol	TABLET	ORAL	20201023	N/A	ANDA	ANDA208884	Zydus Lifesciences Limited	ALBUTEROL SULFATE	2 mg/1	100 TABLET in 1 BOTTLE (70771-1511-1)