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
68382-196-16	68382-196	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.125 mg/1	90 TABLET in 1 BOTTLE (68382-196-16)
68382-197-05	68382-197	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	500 TABLET in 1 BOTTLE (68382-197-05)
68382-197-10	68382-197	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	1000 TABLET in 1 BOTTLE (68382-197-10)
68382-197-16	68382-197	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	90 TABLET in 1 BOTTLE (68382-197-16)
68382-198-05	68382-198	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	500 TABLET in 1 BOTTLE (68382-198-05)
68382-198-10	68382-198	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	1000 TABLET in 1 BOTTLE (68382-198-10)
68382-198-16	68382-198	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.5 mg/1	90 TABLET in 1 BOTTLE (68382-198-16)
68382-199-05	68382-199	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	500 TABLET in 1 BOTTLE (68382-199-05)
68382-199-10	68382-199	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	1000 TABLET in 1 BOTTLE (68382-199-10)
68382-199-16	68382-199	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1 mg/1	90 TABLET in 1 BOTTLE (68382-199-16)
68382-196-10	68382-196	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.125 mg/1	1000 TABLET in 1 BOTTLE (68382-196-10)
68382-196-05	68382-196	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	.125 mg/1	500 TABLET in 1 BOTTLE (68382-196-05)
68382-200-10	68382-200	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	1000 TABLET in 1 BOTTLE (68382-200-10)
68382-200-05	68382-200	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	500 TABLET in 1 BOTTLE (68382-200-05)
68382-200-16	68382-200	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Pharmaceuticals USA Inc.	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	90 TABLET in 1 BOTTLE (68382-200-16)
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)
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)
65841-734-10	65841-734	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE DIHYDROCHLORIDE	PRAMIPEXOLE DIHYDROCHLORIDE	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.125 mg/1	1000 TABLET in 1 BOTTLE (65841-734-10)
65841-735-10	65841-735	HUMAN PRESCRIPTION DRUG	PRAMIPEXOLE DIHYDROCHLORIDE	PRAMIPEXOLE DIHYDROCHLORIDE	TABLET	ORAL	20100710	N/A	ANDA	ANDA078920	Zydus Lifesciences Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.25 mg/1	1000 TABLET in 1 BOTTLE (65841-735-10)