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
31722-907-90	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)
31722-908-05	31722-908	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	500 TABLET in 1 BOTTLE (31722-908-05)
31722-908-10	31722-908	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	1000 TABLET in 1 BOTTLE (31722-908-10)
31722-908-90	31722-908	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	90 TABLET in 1 BOTTLE (31722-908-90)
31722-909-05	31722-909	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	500 TABLET in 1 BOTTLE (31722-909-05)
31722-909-10	31722-909	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	1000 TABLET in 1 BOTTLE (31722-909-10)
31722-909-90	31722-909	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	90 TABLET in 1 BOTTLE (31722-909-90)
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)
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)
31722-906-10	31722-906	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.125 mg/1	1000 TABLET in 1 BOTTLE (31722-906-10)
31722-906-90	31722-906	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE	PRAMIPEXOLE	TABLET	ORAL	20150801	N/A	ANDA	ANDA203855	Camber Pharmaceuticals, Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.125 mg/1	90 TABLET in 1 BOTTLE (31722-906-90)
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)