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
33342-208-07	33342-208	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200824	N/A	ANDA	ANDA206156	Macleods Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.375 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-208-07)
33342-208-12	33342-208	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200824	N/A	ANDA	ANDA206156	Macleods Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.375 mg/1	10 BLISTER PACK in 1 CARTON (33342-208-12) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
33342-212-07	33342-212	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200824	N/A	ANDA	ANDA206156	Macleods Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	3 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-212-07)
33342-212-12	33342-212	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200824	N/A	ANDA	ANDA206156	Macleods Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	3 mg/1	10 BLISTER PACK in 1 CARTON (33342-212-12) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
16714-917-01	16714-917	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190306	N/A	ANDA	ANDA206156	NorthStar RxLLC	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-917-01)
33342-209-07	33342-209	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200824	N/A	ANDA	ANDA206156	Macleods Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-209-07)
33342-209-12	33342-209	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200824	N/A	ANDA	ANDA206156	Macleods Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	.75 mg/1	10 BLISTER PACK in 1 CARTON (33342-209-12) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
33342-213-07	33342-213	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200824	N/A	ANDA	ANDA206156	Macleods Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	3.75 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-213-07)
33342-213-12	33342-213	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200824	N/A	ANDA	ANDA206156	Macleods Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	3.75 mg/1	10 BLISTER PACK in 1 CARTON (33342-213-12) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
16714-918-01	16714-918	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190306	N/A	ANDA	ANDA206156	NorthStar RxLLC	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-918-01)
33342-211-07	33342-211	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200824	N/A	ANDA	ANDA206156	Macleods Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	2.25 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-211-07)
33342-211-12	33342-211	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200824	N/A	ANDA	ANDA206156	Macleods Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	2.25 mg/1	10 BLISTER PACK in 1 CARTON (33342-211-12) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
16714-916-01	16714-916	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190306	N/A	ANDA	ANDA206156	NorthStar RxLLC	PRAMIPEXOLE DIHYDROCHLORIDE	.375 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-916-01)
16714-922-01	16714-922	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190306	N/A	ANDA	ANDA206156	NorthStar RxLLC	PRAMIPEXOLE DIHYDROCHLORIDE	4.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-922-01)
33342-210-07	33342-210	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200824	N/A	ANDA	ANDA206156	Macleods Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-210-07)
33342-210-12	33342-210	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200824	N/A	ANDA	ANDA206156	Macleods Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	1.5 mg/1	10 BLISTER PACK in 1 CARTON (33342-210-12) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
33342-214-07	33342-214	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200824	N/A	ANDA	ANDA206156	Macleods Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	4.5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-214-07)
33342-214-12	33342-214	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20200824	N/A	ANDA	ANDA206156	Macleods Pharmaceuticals Limited	PRAMIPEXOLE DIHYDROCHLORIDE	4.5 mg/1	10 BLISTER PACK in 1 CARTON (33342-214-12) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
16714-919-01	16714-919	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190306	N/A	ANDA	ANDA206156	NorthStar RxLLC	PRAMIPEXOLE DIHYDROCHLORIDE	2.25 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-919-01)
16714-920-01	16714-920	HUMAN PRESCRIPTION DRUG	Pramipexole Dihydrochloride	Pramipexole Dihydrochloride	TABLET, EXTENDED RELEASE	ORAL	20190306	N/A	ANDA	ANDA206156	NorthStar RxLLC	PRAMIPEXOLE DIHYDROCHLORIDE	3 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-920-01)