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=ANDA071321"
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
68071-4770-1 68071-4770 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20190218 N/A ANDA ANDA071321 NuCare Pharmaceuticals,Inc. DIAZEPAM 5 mg/1 10 TABLET in 1 BOTTLE (68071-4770-1)
68071-4770-3 68071-4770 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20190218 N/A ANDA ANDA071321 NuCare Pharmaceuticals,Inc. DIAZEPAM 5 mg/1 30 TABLET in 1 BOTTLE (68071-4770-3)
68071-4770-5 68071-4770 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20190218 N/A ANDA ANDA071321 NuCare Pharmaceuticals,Inc. DIAZEPAM 5 mg/1 15 TABLET in 1 BOTTLE (68071-4770-5)
68071-4770-9 68071-4770 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20190218 N/A ANDA ANDA071321 NuCare Pharmaceuticals,Inc. DIAZEPAM 5 mg/1 90 TABLET in 1 BOTTLE (68071-4770-9)
68071-4922-1 68071-4922 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20190613 N/A ANDA ANDA071321 NuCare Pharmaceuticals,Inc. DIAZEPAM 5 mg/1 10 TABLET in 1 BOTTLE (68071-4922-1)
68071-4922-4 68071-4922 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20190613 N/A ANDA ANDA071321 NuCare Pharmaceuticals,Inc. DIAZEPAM 5 mg/1 8 TABLET in 1 BOTTLE (68071-4922-4)
68071-4922-6 68071-4922 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20190613 N/A ANDA ANDA071321 NuCare Pharmaceuticals,Inc. DIAZEPAM 5 mg/1 6 TABLET in 1 BOTTLE (68071-4922-6)
43063-970-04 43063-970 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20190731 N/A ANDA ANDA071321 PD-Rx Pharmaceuticals, Inc. DIAZEPAM 5 mg/1 4 TABLET in 1 BOTTLE, PLASTIC (43063-970-04)
43063-970-06 43063-970 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20190513 N/A ANDA ANDA071321 PD-Rx Pharmaceuticals, Inc. DIAZEPAM 5 mg/1 6 TABLET in 1 BOTTLE, PLASTIC (43063-970-06)
43063-970-10 43063-970 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20200805 N/A ANDA ANDA071321 PD-Rx Pharmaceuticals, Inc. DIAZEPAM 5 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (43063-970-10)
43063-970-15 43063-970 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20191204 N/A ANDA ANDA071321 PD-Rx Pharmaceuticals, Inc. DIAZEPAM 5 mg/1 15 TABLET in 1 BOTTLE, PLASTIC (43063-970-15)
43063-970-21 43063-970 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20190507 N/A ANDA ANDA071321 PD-Rx Pharmaceuticals, Inc. DIAZEPAM 5 mg/1 21 TABLET in 1 BOTTLE, PLASTIC (43063-970-21)
43063-970-30 43063-970 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20190501 N/A ANDA ANDA071321 PD-Rx Pharmaceuticals, Inc. DIAZEPAM 5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (43063-970-30)
43063-970-60 43063-970 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20191126 N/A ANDA ANDA071321 PD-Rx Pharmaceuticals, Inc. DIAZEPAM 5 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (43063-970-60)
0172-3926-60 0172-3926 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 19861210 N/A ANDA ANDA071321 Teva Pharmaceuticals USA, Inc. DIAZEPAM 5 mg/1 100 TABLET in 1 BOTTLE (0172-3926-60)
0172-3926-70 0172-3926 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 19861210 N/A ANDA ANDA071321 Teva Pharmaceuticals USA, Inc. DIAZEPAM 5 mg/1 500 TABLET in 1 BOTTLE (0172-3926-70)
0172-3926-80 0172-3926 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 19861210 N/A ANDA ANDA071321 Teva Pharmaceuticals USA, Inc. DIAZEPAM 5 mg/1 1000 TABLET in 1 BOTTLE (0172-3926-80)
63187-173-02 63187-173 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20180201 N/A ANDA ANDA071321 Proficient Rx LP DIAZEPAM 5 mg/1 2 TABLET in 1 BOTTLE (63187-173-02)
63187-173-20 63187-173 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20160101 N/A ANDA ANDA071321 Proficient Rx LP DIAZEPAM 5 mg/1 20 TABLET in 1 BOTTLE (63187-173-20)
63187-173-21 63187-173 HUMAN PRESCRIPTION DRUG Diazepam Diazepam TABLET ORAL 20180201 N/A ANDA ANDA071321 Proficient Rx LP DIAZEPAM 5 mg/1 21 TABLET in 1 BOTTLE (63187-173-21)
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