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
63629-8289-1	63629-8289	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20200110	N/A	ANDA	ANDA202633	Bryant Ranch Prepack	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	30 TABLET in 1 BOTTLE (63629-8289-1)
50090-3280-0	50090-3280	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20171127	N/A	ANDA	ANDA202633	A-S Medication Solutions	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	90 TABLET in 1 BOTTLE (50090-3280-0)
50090-2455-0	50090-2455	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20160812	N/A	ANDA	ANDA202633	A-S Medication Solutions	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	30 TABLET in 1 BOTTLE (50090-2455-0)
50090-5036-0	50090-5036	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20200506	N/A	ANDA	ANDA202633	A-S Medication Solutions	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	90 TABLET in 1 BOTTLE (50090-5036-0)
57237-181-99	57237-181	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Rising Pharma Holdings, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	1000 TABLET in 1 BOTTLE (57237-181-99)
57237-182-90	57237-182	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Rising Pharma Holdings, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	90 TABLET in 1 BOTTLE (57237-182-90)
57237-182-99	57237-182	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Rising Pharma Holdings, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	1000 TABLET in 1 BOTTLE (57237-182-99)
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)
57237-180-90	57237-180	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Rising Pharma Holdings, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.125 mg/1	90 TABLET in 1 BOTTLE (57237-180-90)
57237-180-99	57237-180	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Rising Pharma Holdings, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.125 mg/1	1000 TABLET in 1 BOTTLE (57237-180-99)
57237-185-90	57237-185	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Rising Pharma Holdings, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	90 TABLET in 1 BOTTLE (57237-185-90)
57237-185-99	57237-185	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Rising Pharma Holdings, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	1000 TABLET in 1 BOTTLE (57237-185-99)
57237-181-90	57237-181	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Rising Pharma Holdings, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	90 TABLET in 1 BOTTLE (57237-181-90)
57237-184-90	57237-184	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Rising Pharma Holdings, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	90 TABLET in 1 BOTTLE (57237-184-90)
57237-184-99	57237-184	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Rising Pharma Holdings, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	1000 TABLET in 1 BOTTLE (57237-184-99)
65862-604-99	65862-604	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Aurobindo Pharma Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.125 mg/1	1000 TABLET in 1 BOTTLE (65862-604-99)
65862-605-90	65862-605	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Aurobindo Pharma Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	90 TABLET in 1 BOTTLE (65862-605-90)
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)
65862-606-78	65862-606	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Aurobindo Pharma Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	10 BLISTER PACK in 1 CARTON (65862-606-78) / 10 TABLET in 1 BLISTER PACK (65862-606-10)