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
65841-735-16	65841-735	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE DIHYDROCHLORIDE	PRAMIPEXOLE DIHYDROCHLORIDE	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	90 TABLET in 1 BOTTLE (65841-735-16)
65841-736-05	65841-736	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE DIHYDROCHLORIDE	PRAMIPEXOLE DIHYDROCHLORIDE	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	500 TABLET in 1 BOTTLE (65841-736-05)
65841-736-10	65841-736	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE DIHYDROCHLORIDE	PRAMIPEXOLE DIHYDROCHLORIDE	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	1000 TABLET in 1 BOTTLE (65841-736-10)
65841-736-16	65841-736	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE DIHYDROCHLORIDE	PRAMIPEXOLE DIHYDROCHLORIDE	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	90 TABLET in 1 BOTTLE (65841-736-16)
65841-737-05	65841-737	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE DIHYDROCHLORIDE	PRAMIPEXOLE DIHYDROCHLORIDE	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	500 TABLET in 1 BOTTLE (65841-737-05)
65841-737-10	65841-737	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE DIHYDROCHLORIDE	PRAMIPEXOLE DIHYDROCHLORIDE	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	1000 TABLET in 1 BOTTLE (65841-737-10)
65841-737-16	65841-737	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE DIHYDROCHLORIDE	PRAMIPEXOLE DIHYDROCHLORIDE	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	90 TABLET in 1 BOTTLE (65841-737-16)
65841-738-05	65841-738	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE DIHYDROCHLORIDE	PRAMIPEXOLE DIHYDROCHLORIDE	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	500 TABLET in 1 BOTTLE (65841-738-05)
65841-738-10	65841-738	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE DIHYDROCHLORIDE	PRAMIPEXOLE DIHYDROCHLORIDE	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	1000 TABLET in 1 BOTTLE (65841-738-10)
65841-738-16	65841-738	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE DIHYDROCHLORIDE	PRAMIPEXOLE DIHYDROCHLORIDE	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	90 TABLET in 1 BOTTLE (65841-738-16)
68382-440-16	68382-440	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20221123	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	90 TABLET in 1 BOTTLE (68382-440-16)
68382-440-05	68382-440	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20221123	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	500 TABLET in 1 BOTTLE (68382-440-05)
68382-440-10	68382-440	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20221123	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	1000 TABLET in 1 BOTTLE (68382-440-10)
65841-844-05	65841-844	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE DIHYDROCHLORIDE	PRAMIPEXOLE DIHYDROCHLORIDE	TABLET	ORAL	20221130	N/A	ANDA	ANDA078920	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	500 TABLET in 1 BOTTLE (65841-844-05)
65841-844-10	65841-844	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE DIHYDROCHLORIDE	PRAMIPEXOLE DIHYDROCHLORIDE	TABLET	ORAL	20221130	N/A	ANDA	ANDA078920	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	1000 TABLET in 1 BOTTLE (65841-844-10)
65841-844-16	65841-844	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE DIHYDROCHLORIDE	PRAMIPEXOLE DIHYDROCHLORIDE	TABLET	ORAL	20221123	N/A	ANDA	ANDA078920	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	90 TABLET in 1 BOTTLE (65841-844-16)