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=ANDA203855"
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
60429-085-90 60429-085 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 Golden State Medical Supply, Inc. PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 90 TABLET in 1 BOTTLE (60429-085-90)
60429-086-90 60429-086 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 Golden State Medical Supply, Inc. PRAMIPEXOLE DIHYDROCHLORIDE .25 mg/1 90 TABLET in 1 BOTTLE (60429-086-90)
60429-087-90 60429-087 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 Golden State Medical Supply, Inc. PRAMIPEXOLE DIHYDROCHLORIDE .5 mg/1 90 TABLET in 1 BOTTLE (60429-087-90)
60429-089-90 60429-089 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 Golden State Medical Supply, Inc. PRAMIPEXOLE DIHYDROCHLORIDE 1 mg/1 90 TABLET in 1 BOTTLE (60429-089-90)
60429-090-90 60429-090 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 Golden State Medical Supply, Inc. PRAMIPEXOLE DIHYDROCHLORIDE 1.5 mg/1 90 TABLET in 1 BOTTLE (60429-090-90)
50228-126-10 50228-126 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 ScieGen Pharmaceuticals Inc PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 1000 TABLET in 1 BOTTLE (50228-126-10)
50228-126-90 50228-126 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 ScieGen Pharmaceuticals Inc PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 90 TABLET in 1 BOTTLE (50228-126-90)
50228-127-10 50228-127 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 ScieGen Pharmaceuticals Inc PRAMIPEXOLE DIHYDROCHLORIDE .25 mg/1 1000 TABLET in 1 BOTTLE (50228-127-10)
50228-127-90 50228-127 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 ScieGen Pharmaceuticals Inc PRAMIPEXOLE DIHYDROCHLORIDE .25 mg/1 90 TABLET in 1 BOTTLE (50228-127-90)
50228-128-10 50228-128 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 ScieGen Pharmaceuticals Inc PRAMIPEXOLE DIHYDROCHLORIDE .5 mg/1 1000 TABLET in 1 BOTTLE (50228-128-10)
50228-128-90 50228-128 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 ScieGen Pharmaceuticals Inc PRAMIPEXOLE DIHYDROCHLORIDE .5 mg/1 90 TABLET in 1 BOTTLE (50228-128-90)
50228-129-10 50228-129 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 ScieGen Pharmaceuticals Inc PRAMIPEXOLE DIHYDROCHLORIDE .75 mg/1 1000 TABLET in 1 BOTTLE (50228-129-10)
50228-129-90 50228-129 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 ScieGen Pharmaceuticals Inc PRAMIPEXOLE DIHYDROCHLORIDE .75 mg/1 90 TABLET in 1 BOTTLE (50228-129-90)
50228-130-10 50228-130 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 ScieGen Pharmaceuticals Inc PRAMIPEXOLE DIHYDROCHLORIDE 1 mg/1 1000 TABLET in 1 BOTTLE (50228-130-10)
50228-130-90 50228-130 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 ScieGen Pharmaceuticals Inc PRAMIPEXOLE DIHYDROCHLORIDE 1 mg/1 90 TABLET in 1 BOTTLE (50228-130-90)
50228-131-10 50228-131 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 ScieGen Pharmaceuticals Inc PRAMIPEXOLE DIHYDROCHLORIDE 1.5 mg/1 1000 TABLET in 1 BOTTLE (50228-131-10)
50228-131-90 50228-131 HUMAN PRESCRIPTION DRUG Pramipexole Dihydrochloride Pramipexole Dihydrochloride TABLET ORAL 20141029 N/A ANDA ANDA203855 ScieGen Pharmaceuticals Inc PRAMIPEXOLE DIHYDROCHLORIDE 1.5 mg/1 90 TABLET in 1 BOTTLE (50228-131-90)
31722-906-05 31722-906 HUMAN PRESCRIPTION DRUG PRAMIPEXOLE PRAMIPEXOLE TABLET ORAL 20150801 N/A ANDA ANDA203855 Camber Pharmaceuticals, Inc. PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 500 TABLET in 1 BOTTLE (31722-906-05)
31722-906-10 31722-906 HUMAN PRESCRIPTION DRUG PRAMIPEXOLE PRAMIPEXOLE TABLET ORAL 20150801 N/A ANDA ANDA203855 Camber Pharmaceuticals, Inc. PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 1000 TABLET in 1 BOTTLE (31722-906-10)
31722-906-90 31722-906 HUMAN PRESCRIPTION DRUG PRAMIPEXOLE PRAMIPEXOLE TABLET ORAL 20150801 N/A ANDA ANDA203855 Camber Pharmaceuticals, Inc. PRAMIPEXOLE DIHYDROCHLORIDE .125 mg/1 90 TABLET in 1 BOTTLE (31722-906-90)
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