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
70771-1333-4	70771-1333	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180424	N/A	ANDA	ANDA202891	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	3.75 mg/1	10 BLISTER PACK in 1 CARTON (70771-1333-4) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70771-1333-2)
70771-1334-3	70771-1334	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180424	N/A	ANDA	ANDA202891	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	4.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1334-3)
70771-1334-4	70771-1334	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180424	N/A	ANDA	ANDA202891	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	4.5 mg/1	10 BLISTER PACK in 1 CARTON (70771-1334-4) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70771-1334-2)
68382-875-77	68382-875	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180424	N/A	ANDA	ANDA202891	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	3.75 mg/1	10 BLISTER PACK in 1 CARTON (68382-875-77) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68382-875-30)
70771-1328-4	70771-1328	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180424	N/A	ANDA	ANDA202891	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.375 mg/1	10 BLISTER PACK in 1 CARTON (70771-1328-4) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70771-1328-2)
70771-1328-3	70771-1328	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20180424	N/A	ANDA	ANDA202891	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.375 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1328-3)