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=ANDA207011"
符合检索条件的记录共 13 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
29300-209-10 29300-209 HUMAN PRESCRIPTION DRUG pramipexole dihydrochloride pramipexole dihydrochloride TABLET ORAL 20190301 N/A ANDA ANDA207011 Unichem Pharmaceuticals (USA), Inc. PRAMIPEXOLE DIHYDROCHLORIDE .5 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (29300-209-10)
29300-209-19 29300-209 HUMAN PRESCRIPTION DRUG pramipexole dihydrochloride pramipexole dihydrochloride TABLET ORAL 20190301 N/A ANDA ANDA207011 Unichem Pharmaceuticals (USA), Inc. PRAMIPEXOLE DIHYDROCHLORIDE .5 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (29300-209-19)
29300-207-10 29300-207 HUMAN PRESCRIPTION DRUG pramipexole dihydrochloride pramipexole dihydrochloride TABLET ORAL 20190301 N/A ANDA ANDA207011 Unichem Pharmaceuticals (USA), Inc. PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (29300-207-10)
29300-207-16 29300-207 HUMAN PRESCRIPTION DRUG pramipexole dihydrochloride pramipexole dihydrochloride TABLET ORAL 20190301 N/A ANDA ANDA207011 Unichem Pharmaceuticals (USA), Inc. PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (29300-207-16)
29300-207-19 29300-207 HUMAN PRESCRIPTION DRUG pramipexole dihydrochloride pramipexole dihydrochloride TABLET ORAL 20190301 N/A ANDA ANDA207011 Unichem Pharmaceuticals (USA), Inc. PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (29300-207-19)
29300-211-10 29300-211 HUMAN PRESCRIPTION DRUG pramipexole dihydrochloride pramipexole dihydrochloride TABLET ORAL 20190301 N/A ANDA ANDA207011 Unichem Pharmaceuticals (USA), Inc. PRAMIPEXOLE DIHYDROCHLORIDE 1.5 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (29300-211-10)
29300-211-19 29300-211 HUMAN PRESCRIPTION DRUG pramipexole dihydrochloride pramipexole dihydrochloride TABLET ORAL 20190301 N/A ANDA ANDA207011 Unichem Pharmaceuticals (USA), Inc. PRAMIPEXOLE DIHYDROCHLORIDE 1.5 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (29300-211-19)
29300-270-10 29300-270 HUMAN PRESCRIPTION DRUG pramipexole dihydrochloride pramipexole dihydrochloride TABLET ORAL 20190301 N/A ANDA ANDA207011 Unichem Pharmaceuticals (USA), Inc. PRAMIPEXOLE DIHYDROCHLORIDE .75 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (29300-270-10)
29300-270-19 29300-270 HUMAN PRESCRIPTION DRUG pramipexole dihydrochloride pramipexole dihydrochloride TABLET ORAL 20190301 N/A ANDA ANDA207011 Unichem Pharmaceuticals (USA), Inc. PRAMIPEXOLE DIHYDROCHLORIDE .75 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (29300-270-19)
29300-210-10 29300-210 HUMAN PRESCRIPTION DRUG pramipexole dihydrochloride pramipexole dihydrochloride TABLET ORAL 20190301 N/A ANDA ANDA207011 Unichem Pharmaceuticals (USA), Inc. PRAMIPEXOLE DIHYDROCHLORIDE 1 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (29300-210-10)
29300-210-19 29300-210 HUMAN PRESCRIPTION DRUG pramipexole dihydrochloride pramipexole dihydrochloride TABLET ORAL 20190301 N/A ANDA ANDA207011 Unichem Pharmaceuticals (USA), Inc. PRAMIPEXOLE DIHYDROCHLORIDE 1 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (29300-210-19)
29300-208-10 29300-208 HUMAN PRESCRIPTION DRUG pramipexole dihydrochloride pramipexole dihydrochloride TABLET ORAL 20190301 N/A ANDA ANDA207011 Unichem Pharmaceuticals (USA), Inc. PRAMIPEXOLE DIHYDROCHLORIDE .25 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (29300-208-10)
29300-208-19 29300-208 HUMAN PRESCRIPTION DRUG pramipexole dihydrochloride pramipexole dihydrochloride TABLET ORAL 20190301 N/A ANDA ANDA207011 Unichem Pharmaceuticals (USA), Inc. PRAMIPEXOLE DIHYDROCHLORIDE .25 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (29300-208-19)
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