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
46708-004-90	46708-004	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20160322	N/A	ANDA	ANDA078894	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	90 TABLET in 1 BOTTLE (46708-004-90)
46708-005-90	46708-005	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20160322	N/A	ANDA	ANDA078894	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	90 TABLET in 1 BOTTLE (46708-005-90)
46708-006-90	46708-006	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20160322	N/A	ANDA	ANDA078894	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	90 TABLET in 1 BOTTLE (46708-006-90)
46708-007-90	46708-007	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20160322	N/A	ANDA	ANDA078894	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	90 TABLET in 1 BOTTLE (46708-007-90)
46708-612-90	46708-612	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20160322	N/A	ANDA	ANDA078894	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	90 TABLET in 1 BOTTLE (46708-612-90)
46708-613-90	46708-613	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20160322	N/A	ANDA	ANDA078894	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	90 TABLET in 1 BOTTLE (46708-613-90)
46708-614-90	46708-614	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20160322	N/A	ANDA	ANDA078894	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	90 TABLET in 1 BOTTLE (46708-614-90)
46708-615-90	46708-615	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20160322	N/A	ANDA	ANDA078894	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	90 TABLET in 1 BOTTLE (46708-615-90)
62332-004-90	62332-004	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20160322	N/A	ANDA	ANDA078894	Alembic Pharmaceuticals Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	90 TABLET in 1 BOTTLE (62332-004-90)
62332-005-90	62332-005	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20160322	N/A	ANDA	ANDA078894	Alembic Pharmaceuticals Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	90 TABLET in 1 BOTTLE (62332-005-90)
62332-006-90	62332-006	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20160322	N/A	ANDA	ANDA078894	Alembic Pharmaceuticals Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	90 TABLET in 1 BOTTLE (62332-006-90)
62332-007-90	62332-007	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20160322	N/A	ANDA	ANDA078894	Alembic Pharmaceuticals Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	90 TABLET in 1 BOTTLE (62332-007-90)
62332-003-90	62332-003	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20160322	N/A	ANDA	ANDA078894	Alembic Pharmaceuticals Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.125 mg/1	90 TABLET in 1 BOTTLE (62332-003-90)
46708-611-90	46708-611	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20160322	N/A	ANDA	ANDA078894	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.125 mg/1	90 TABLET in 1 BOTTLE (46708-611-90)
46708-003-90	46708-003	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20160322	N/A	ANDA	ANDA078894	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.125 mg/1	90 TABLET in 1 BOTTLE (46708-003-90)