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)
检索条件:" 注册申请号=ANDA206156"
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
33342-209-12 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
33342-210-07 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
33342-211-07 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
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
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
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
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)
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)
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)
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)
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)
33342-208-12 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
33342-208-07 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)
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)
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