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
46708-574-30	46708-574	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190103	N/A	ANDA	ANDA204518	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.375 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-574-30)
46708-575-30	46708-575	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190103	N/A	ANDA	ANDA204518	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-575-30)
46708-576-30	46708-576	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190103	N/A	ANDA	ANDA204518	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-576-30)
46708-577-30	46708-577	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190103	N/A	ANDA	ANDA204518	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	2.25 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-577-30)
46708-578-30	46708-578	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190103	N/A	ANDA	ANDA204518	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	3 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-578-30)
46708-579-30	46708-579	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190103	N/A	ANDA	ANDA204518	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	3.75 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-579-30)
46708-580-30	46708-580	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190103	N/A	ANDA	ANDA204518	Alembic Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	4.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-580-30)
62332-154-30	62332-154	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190103	N/A	ANDA	ANDA204518	Alembic Pharmaceuticals Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.375 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-154-30)
62332-155-30	62332-155	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190103	N/A	ANDA	ANDA204518	Alembic Pharmaceuticals Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-155-30)
62332-156-30	62332-156	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190103	N/A	ANDA	ANDA204518	Alembic Pharmaceuticals Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-156-30)
62332-157-30	62332-157	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190103	N/A	ANDA	ANDA204518	Alembic Pharmaceuticals Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	2.25 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-157-30)
62332-158-30	62332-158	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190103	N/A	ANDA	ANDA204518	Alembic Pharmaceuticals Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	3 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-158-30)
62332-159-30	62332-159	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190103	N/A	ANDA	ANDA204518	Alembic Pharmaceuticals Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	4.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-159-30)
62332-160-30	62332-160	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190103	N/A	ANDA	ANDA204518	Alembic Pharmaceuticals Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	3.75 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-160-30)