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
55111-614-30	55111-614	HUMAN PRESCRIPTION DRUG	Pramipexole dihydrochloride	Pramipexole dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20150814	N/A	ANDA	ANDA203354	Dr. Reddy's Laboratories Limited	PRAMIPEXOLE DIHYDROCHLORIDE	3 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-614-30)
55111-615-30	55111-615	HUMAN PRESCRIPTION DRUG	Pramipexole dihydrochloride	Pramipexole dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20150814	N/A	ANDA	ANDA203354	Dr. Reddy's Laboratories Limited	PRAMIPEXOLE DIHYDROCHLORIDE	4.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-615-30)
55111-613-30	55111-613	HUMAN PRESCRIPTION DRUG	Pramipexole dihydrochloride	Pramipexole dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20150814	N/A	ANDA	ANDA203354	Dr. Reddy's Laboratories Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-613-30)
55111-612-30	55111-612	HUMAN PRESCRIPTION DRUG	Pramipexole dihydrochloride	Pramipexole dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20150814	N/A	ANDA	ANDA203354	Dr. Reddy's Laboratories Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-612-30)
55111-611-30	55111-611	HUMAN PRESCRIPTION DRUG	Pramipexole dihydrochloride	Pramipexole dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20150814	N/A	ANDA	ANDA203354	Dr. Reddy's Laboratories Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.375 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-611-30)