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=ANDA205064"
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
31722-921-01 31722-921 HUMAN PRESCRIPTION DRUG ARIPIPRAZOLE aripiprazole TABLET ORAL 20170801 N/A ANDA ANDA205064 Camber Pharmaceuticals, Inc. ARIPIPRAZOLE 10 mg/1 100 TABLET in 1 BOTTLE (31722-921-01)
31722-921-30 31722-921 HUMAN PRESCRIPTION DRUG ARIPIPRAZOLE aripiprazole TABLET ORAL 20170801 N/A ANDA ANDA205064 Camber Pharmaceuticals, Inc. ARIPIPRAZOLE 10 mg/1 30 TABLET in 1 BOTTLE (31722-921-30)
31722-922-01 31722-922 HUMAN PRESCRIPTION DRUG ARIPIPRAZOLE aripiprazole TABLET ORAL 20170801 N/A ANDA ANDA205064 Camber Pharmaceuticals, Inc. ARIPIPRAZOLE 15 mg/1 100 TABLET in 1 BOTTLE (31722-922-01)
31722-922-30 31722-922 HUMAN PRESCRIPTION DRUG ARIPIPRAZOLE aripiprazole TABLET ORAL 20170801 N/A ANDA ANDA205064 Camber Pharmaceuticals, Inc. ARIPIPRAZOLE 15 mg/1 30 TABLET in 1 BOTTLE (31722-922-30)
31722-923-01 31722-923 HUMAN PRESCRIPTION DRUG ARIPIPRAZOLE aripiprazole TABLET ORAL 20170801 N/A ANDA ANDA205064 Camber Pharmaceuticals, Inc. ARIPIPRAZOLE 20 mg/1 100 TABLET in 1 BOTTLE (31722-923-01)
31722-923-30 31722-923 HUMAN PRESCRIPTION DRUG ARIPIPRAZOLE aripiprazole TABLET ORAL 20170801 N/A ANDA ANDA205064 Camber Pharmaceuticals, Inc. ARIPIPRAZOLE 20 mg/1 30 TABLET in 1 BOTTLE (31722-923-30)
31722-924-01 31722-924 HUMAN PRESCRIPTION DRUG ARIPIPRAZOLE aripiprazole TABLET ORAL 20170801 N/A ANDA ANDA205064 Camber Pharmaceuticals, Inc. ARIPIPRAZOLE 30 mg/1 100 TABLET in 1 BOTTLE (31722-924-01)
31722-924-30 31722-924 HUMAN PRESCRIPTION DRUG ARIPIPRAZOLE aripiprazole TABLET ORAL 20170801 N/A ANDA ANDA205064 Camber Pharmaceuticals, Inc. ARIPIPRAZOLE 30 mg/1 30 TABLET in 1 BOTTLE (31722-924-30)
71335-1892-1 71335-1892 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20210629 N/A ANDA ANDA205064 Bryant Ranch Prepack ARIPIPRAZOLE 2 mg/1 30 TABLET in 1 BOTTLE (71335-1892-1)
71335-1892-2 71335-1892 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20210629 N/A ANDA ANDA205064 Bryant Ranch Prepack ARIPIPRAZOLE 2 mg/1 28 TABLET in 1 BOTTLE (71335-1892-2)
71335-1892-3 71335-1892 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20210629 N/A ANDA ANDA205064 Bryant Ranch Prepack ARIPIPRAZOLE 2 mg/1 90 TABLET in 1 BOTTLE (71335-1892-3)
71335-1892-4 71335-1892 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20210629 N/A ANDA ANDA205064 Bryant Ranch Prepack ARIPIPRAZOLE 2 mg/1 60 TABLET in 1 BOTTLE (71335-1892-4)
71335-1893-1 71335-1893 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20210630 N/A ANDA ANDA205064 Bryant Ranch Prepack ARIPIPRAZOLE 5 mg/1 30 TABLET in 1 BOTTLE (71335-1893-1)
71335-1893-2 71335-1893 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20240405 N/A ANDA ANDA205064 Bryant Ranch Prepack ARIPIPRAZOLE 5 mg/1 28 TABLET in 1 BOTTLE (71335-1893-2)
71335-1893-3 71335-1893 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20210716 N/A ANDA ANDA205064 Bryant Ranch Prepack ARIPIPRAZOLE 5 mg/1 90 TABLET in 1 BOTTLE (71335-1893-3)
71335-1893-4 71335-1893 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20210719 N/A ANDA ANDA205064 Bryant Ranch Prepack ARIPIPRAZOLE 5 mg/1 60 TABLET in 1 BOTTLE (71335-1893-4)
71335-1893-5 71335-1893 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20240405 N/A ANDA ANDA205064 Bryant Ranch Prepack ARIPIPRAZOLE 5 mg/1 120 TABLET in 1 BOTTLE (71335-1893-5)
71335-1893-6 71335-1893 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20240405 N/A ANDA ANDA205064 Bryant Ranch Prepack ARIPIPRAZOLE 5 mg/1 15 TABLET in 1 BOTTLE (71335-1893-6)
68071-3471-3 68071-3471 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20230726 N/A ANDA ANDA205064 NuCare Pharmaceuticals,Inc. ARIPIPRAZOLE 5 mg/1 30 TABLET in 1 BOTTLE (68071-3471-3)
63739-069-33 63739-069 HUMAN PRESCRIPTION DRUG Aripiprazole Aripiprazole TABLET ORAL 20211109 N/A ANDA ANDA205064 McKesson Corporation dba SKY Packaging ARIPIPRAZOLE 2 mg/1 3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-069-33) / 10 TABLET in 1 BLISTER PACK
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase