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
71335-1808-2	71335-1808	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20210419	N/A	ANDA	ANDA202633	Bryant Ranch Prepack	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	30 TABLET in 1 BOTTLE (71335-1808-2)
71335-1808-3	71335-1808	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20211229	N/A	ANDA	ANDA202633	Bryant Ranch Prepack	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	60 TABLET in 1 BOTTLE (71335-1808-3)
57237-183-90	57237-183	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Rising Pharma Holdings, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	90 TABLET in 1 BOTTLE (57237-183-90)
57237-183-99	57237-183	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Rising Pharma Holdings, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	1000 TABLET in 1 BOTTLE (57237-183-99)