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
65862-605-99	65862-605	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Aurobindo Pharma Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	1000 TABLET in 1 BOTTLE (65862-605-99)
65862-608-78	65862-608	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Aurobindo Pharma Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	10 BLISTER PACK in 1 CARTON (65862-608-78) / 10 TABLET in 1 BLISTER PACK (65862-608-10)
65862-608-99	65862-608	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Aurobindo Pharma Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	1000 TABLET in 1 BOTTLE (65862-608-99)
65862-609-78	65862-609	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Aurobindo Pharma Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	10 BLISTER PACK in 1 CARTON (65862-609-78) / 10 TABLET in 1 BLISTER PACK (65862-609-10)