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
71205-898-55	71205-898	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20210730	N/A	ANDA	ANDA207046	Proficient Rx LP	ALBUTEROL SULFATE	2 mg/1	500 TABLET in 1 BOTTLE (71205-898-55)
71205-898-60	71205-898	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20210730	N/A	ANDA	ANDA207046	Proficient Rx LP	ALBUTEROL SULFATE	2 mg/1	60 TABLET in 1 BOTTLE (71205-898-60)
71205-898-90	71205-898	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20210730	N/A	ANDA	ANDA207046	Proficient Rx LP	ALBUTEROL SULFATE	2 mg/1	90 TABLET in 1 BOTTLE (71205-898-90)
71205-899-00	71205-899	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20210730	N/A	ANDA	ANDA207046	Proficient Rx LP	ALBUTEROL SULFATE	4 mg/1	100 TABLET in 1 BOTTLE (71205-899-00)
71205-899-11	71205-899	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20210730	N/A	ANDA	ANDA207046	Proficient Rx LP	ALBUTEROL SULFATE	4 mg/1	1000 TABLET in 1 BOTTLE (71205-899-11)
71205-899-30	71205-899	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20210730	N/A	ANDA	ANDA207046	Proficient Rx LP	ALBUTEROL SULFATE	4 mg/1	30 TABLET in 1 BOTTLE (71205-899-30)
71205-899-55	71205-899	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20210730	N/A	ANDA	ANDA207046	Proficient Rx LP	ALBUTEROL SULFATE	4 mg/1	500 TABLET in 1 BOTTLE (71205-899-55)
71205-899-60	71205-899	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20210730	N/A	ANDA	ANDA207046	Proficient Rx LP	ALBUTEROL SULFATE	4 mg/1	60 TABLET in 1 BOTTLE (71205-899-60)
71205-899-90	71205-899	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20210730	N/A	ANDA	ANDA207046	Proficient Rx LP	ALBUTEROL SULFATE	4 mg/1	90 TABLET in 1 BOTTLE (71205-899-90)
64980-442-01	64980-442	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20180629	N/A	ANDA	ANDA207046	Rising Pharmaceuticals, Inc.	ALBUTEROL SULFATE	2 mg/1	100 TABLET in 1 BOTTLE (64980-442-01)
64980-442-50	64980-442	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20180629	N/A	ANDA	ANDA207046	Rising Pharmaceuticals, Inc.	ALBUTEROL SULFATE	2 mg/1	500 TABLET in 1 BOTTLE (64980-442-50)
64980-443-01	64980-443	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20180629	N/A	ANDA	ANDA207046	Rising Pharmaceuticals, Inc.	ALBUTEROL SULFATE	4 mg/1	100 TABLET in 1 BOTTLE (64980-443-01)
64980-443-50	64980-443	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20180629	N/A	ANDA	ANDA207046	Rising Pharmaceuticals, Inc.	ALBUTEROL SULFATE	4 mg/1	500 TABLET in 1 BOTTLE (64980-443-50)
71205-898-30	71205-898	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20210730	N/A	ANDA	ANDA207046	Proficient Rx LP	ALBUTEROL SULFATE	2 mg/1	30 TABLET in 1 BOTTLE (71205-898-30)
71205-898-11	71205-898	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20210730	N/A	ANDA	ANDA207046	Proficient Rx LP	ALBUTEROL SULFATE	2 mg/1	1000 TABLET in 1 BOTTLE (71205-898-11)
71205-898-00	71205-898	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20210730	N/A	ANDA	ANDA207046	Proficient Rx LP	ALBUTEROL SULFATE	2 mg/1	100 TABLET in 1 BOTTLE (71205-898-00)
63629-2611-1	63629-2611	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20220718	N/A	ANDA	ANDA207046	Bryant Ranch Prepack	ALBUTEROL SULFATE	4 mg/1	20 TABLET in 1 BOTTLE (63629-2611-1)
63629-2611-2	63629-2611	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20220718	N/A	ANDA	ANDA207046	Bryant Ranch Prepack	ALBUTEROL SULFATE	4 mg/1	30 TABLET in 1 BOTTLE (63629-2611-2)
63629-2611-3	63629-2611	HUMAN PRESCRIPTION DRUG	Albuterol	albuterol	TABLET	ORAL	20220718	N/A	ANDA	ANDA207046	Bryant Ranch Prepack	ALBUTEROL SULFATE	4 mg/1	60 TABLET in 1 BOTTLE (63629-2611-3)