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
71335-1504-1	71335-1504	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20211228	N/A	ANDA	ANDA202633	Bryant Ranch Prepack	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	30 TABLET in 1 BOTTLE (71335-1504-1)
71335-1504-2	71335-1504	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20200211	N/A	ANDA	ANDA202633	Bryant Ranch Prepack	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	90 TABLET in 1 BOTTLE (71335-1504-2)
65862-605-78	65862-605	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Aurobindo Pharma Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	10 BLISTER PACK in 1 CARTON (65862-605-78) / 10 TABLET in 1 BLISTER PACK (65862-605-10)
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)
65862-609-78	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)
65862-609-90	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	90 TABLET in 1 BOTTLE (65862-609-90)
65862-609-99	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	1000 TABLET in 1 BOTTLE (65862-609-99)
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)
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)
65862-607-78	65862-607	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Aurobindo Pharma Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	10 BLISTER PACK in 1 CARTON (65862-607-78) / 10 TABLET in 1 BLISTER PACK (65862-607-10)
65862-607-90	65862-607	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Aurobindo Pharma Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	90 TABLET in 1 BOTTLE (65862-607-90)
65862-607-99	65862-607	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20121026	N/A	ANDA	ANDA202633	Aurobindo Pharma Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	1000 TABLET in 1 BOTTLE (65862-607-99)
71335-1877-1	71335-1877	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20210528	N/A	ANDA	ANDA202633	Bryant Ranch Prepack	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	90 TABLET in 1 BOTTLE (71335-1877-1)
71335-1877-2	71335-1877	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20211229	N/A	ANDA	ANDA202633	Bryant Ranch Prepack	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	30 TABLET in 1 BOTTLE (71335-1877-2)
71335-1877-3	71335-1877	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20211229	N/A	ANDA	ANDA202633	Bryant Ranch Prepack	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	60 TABLET in 1 BOTTLE (71335-1877-3)
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)