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=ANDA209582"
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
70710-1121-1 70710-1121 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20180111 N/A ANDA ANDA209582 Zydus Pharmaceuticals USA Inc. DOXYCYCLINE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1121-1)
70710-1122-1 70710-1122 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20180111 N/A ANDA ANDA209582 Zydus Pharmaceuticals USA Inc. DOXYCYCLINE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1122-1)
70710-1123-7 70710-1123 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20180111 N/A ANDA ANDA209582 Zydus Pharmaceuticals USA Inc. DOXYCYCLINE 100 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (70710-1123-7)
70710-1123-8 70710-1123 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20180111 N/A ANDA ANDA209582 Zydus Pharmaceuticals USA Inc. DOXYCYCLINE 100 mg/1 250 TABLET, FILM COATED in 1 BOTTLE (70710-1123-8)
70710-1124-1 70710-1124 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20180111 N/A ANDA ANDA209582 Zydus Pharmaceuticals USA Inc. DOXYCYCLINE 150 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1124-1)
70710-1124-3 70710-1124 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20180111 N/A ANDA ANDA209582 Zydus Pharmaceuticals USA Inc. DOXYCYCLINE 150 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70710-1124-3)
82804-028-06 82804-028 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20231017 N/A ANDA ANDA209582 Proficient Rx LP DOXYCYCLINE 100 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (82804-028-06)
82804-028-14 82804-028 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20231017 N/A ANDA ANDA209582 Proficient Rx LP DOXYCYCLINE 100 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (82804-028-14)
82804-028-20 82804-028 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20231017 N/A ANDA ANDA209582 Proficient Rx LP DOXYCYCLINE 100 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (82804-028-20)
82804-028-30 82804-028 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20231017 N/A ANDA ANDA209582 Proficient Rx LP DOXYCYCLINE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (82804-028-30)
82804-028-60 82804-028 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20231017 N/A ANDA ANDA209582 Proficient Rx LP DOXYCYCLINE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (82804-028-60)
82804-028-90 82804-028 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20231017 N/A ANDA ANDA209582 Proficient Rx LP DOXYCYCLINE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (82804-028-90)
70771-1006-1 70771-1006 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20180111 N/A ANDA ANDA209582 Zydus Lifesciences Limited DOXYCYCLINE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1006-1)
70771-1007-1 70771-1007 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20180111 N/A ANDA ANDA209582 Zydus Lifesciences Limited DOXYCYCLINE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1007-1)
70771-1008-7 70771-1008 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20180111 N/A ANDA ANDA209582 Zydus Lifesciences Limited DOXYCYCLINE 100 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (70771-1008-7)
70771-1008-8 70771-1008 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20180111 N/A ANDA ANDA209582 Zydus Lifesciences Limited DOXYCYCLINE 100 mg/1 250 TABLET, FILM COATED in 1 BOTTLE (70771-1008-8)
70771-1009-1 70771-1009 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20180111 N/A ANDA ANDA209582 Zydus Lifesciences Limited DOXYCYCLINE 150 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1009-1)
70771-1009-3 70771-1009 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline TABLET, FILM COATED ORAL 20180111 N/A ANDA ANDA209582 Zydus Lifesciences Limited DOXYCYCLINE 150 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70771-1009-3)
80425-0319-1 80425-0319 HUMAN PRESCRIPTION DRUG Doxycycline Monohydrate Doxycycline Monohydrate TABLET, FILM COATED ORAL 20230411 N/A ANDA ANDA209582 Advanced Rx Pharmacy of Tennessee, LLC DOXYCYCLINE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0319-1)
80425-0319-2 80425-0319 HUMAN PRESCRIPTION DRUG Doxycycline Monohydrate Doxycycline Monohydrate TABLET, FILM COATED ORAL 20230411 N/A ANDA ANDA209582 Advanced Rx Pharmacy of Tennessee, LLC DOXYCYCLINE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0319-2)
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