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
31722-910-05	31722-910	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	500 TABLET in 1 BOTTLE (31722-910-05)
31722-910-10	31722-910	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	1000 TABLET in 1 BOTTLE (31722-910-10)
31722-910-90	31722-910	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	90 TABLET in 1 BOTTLE (31722-910-90)
50228-128-10	50228-128	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20141029	N/A	ANDA	ANDA203855	ScieGen Pharmaceuticals Inc	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	1000 TABLET in 1 BOTTLE (50228-128-10)
50228-128-90	50228-128	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20141029	N/A	ANDA	ANDA203855	ScieGen Pharmaceuticals Inc	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	90 TABLET in 1 BOTTLE (50228-128-90)
60429-086-90	60429-086	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20250407	N/A	ANDA	ANDA203855	Golden State Medical Supply, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	90 TABLET in 1 BOTTLE (60429-086-90)
60429-090-90	60429-090	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20250407	N/A	ANDA	ANDA203855	Golden State Medical Supply, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	90 TABLET in 1 BOTTLE (60429-090-90)
31722-907-05	31722-907	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	500 TABLET in 1 BOTTLE (31722-907-05)
31722-907-10	31722-907	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	1000 TABLET in 1 BOTTLE (31722-907-10)
31722-907-90	31722-907	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	90 TABLET in 1 BOTTLE (31722-907-90)
31722-911-05	31722-911	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	500 TABLET in 1 BOTTLE (31722-911-05)
31722-911-10	31722-911	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	1000 TABLET in 1 BOTTLE (31722-911-10)
31722-911-90	31722-911	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	90 TABLET in 1 BOTTLE (31722-911-90)
50228-129-10	50228-129	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20141029	N/A	ANDA	ANDA203855	ScieGen Pharmaceuticals Inc	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	1000 TABLET in 1 BOTTLE (50228-129-10)
50228-129-90	50228-129	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20141029	N/A	ANDA	ANDA203855	ScieGen Pharmaceuticals Inc	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	90 TABLET in 1 BOTTLE (50228-129-90)
60429-087-90	60429-087	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20250407	N/A	ANDA	ANDA203855	Golden State Medical Supply, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	90 TABLET in 1 BOTTLE (60429-087-90)