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=ANDA090796"
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
63187-451-30 63187-451 HUMAN PRESCRIPTION DRUG ibuprofen ibuprofen TABLET ORAL 20190101 N/A ANDA ANDA090796 Proficient Rx LP IBUPROFEN 600 mg/1 30 TABLET in 1 BOTTLE (63187-451-30)
63187-451-40 63187-451 HUMAN PRESCRIPTION DRUG ibuprofen ibuprofen TABLET ORAL 20190101 N/A ANDA ANDA090796 Proficient Rx LP IBUPROFEN 600 mg/1 40 TABLET in 1 BOTTLE (63187-451-40)
63187-451-60 63187-451 HUMAN PRESCRIPTION DRUG ibuprofen ibuprofen TABLET ORAL 20190101 N/A ANDA ANDA090796 Proficient Rx LP IBUPROFEN 600 mg/1 60 TABLET in 1 BOTTLE (63187-451-60)
63187-451-90 63187-451 HUMAN PRESCRIPTION DRUG ibuprofen ibuprofen TABLET ORAL 20190101 N/A ANDA ANDA090796 Proficient Rx LP IBUPROFEN 600 mg/1 90 TABLET in 1 BOTTLE (63187-451-90)
68071-3362-0 68071-3362 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (68071-3362-0)
68071-3362-1 68071-3362 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (68071-3362-1)
68071-3362-2 68071-3362 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68071-3362-2)
68071-3362-3 68071-3362 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3362-3)
68071-3362-4 68071-3362 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (68071-3362-4)
73086-212-01 73086-212 HUMAN PRESCRIPTION DRUG ibuprofen ibuprofen TABLET ORAL 20240320 N/A ANDA ANDA090796 SKYA HEALTH, LLC IBUPROFEN 800 mg/1 100 TABLET in 1 BOTTLE (73086-212-01)
80425-0132-1 80425-0132 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 Advanced Rx Pharmacy of Tennessee, LLC IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0132-1)
80425-0132-2 80425-0132 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 Advanced Rx Pharmacy of Tennessee, LLC IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0132-2)
80425-0132-3 80425-0132 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 Advanced Rx Pharmacy of Tennessee, LLC IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (80425-0132-3)
51655-474-20 51655-474 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20201119 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 600 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-20)
51655-474-25 51655-474 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20201113 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-25)
51655-474-26 51655-474 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220621 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-26)
51655-474-51 51655-474 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210208 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 600 mg/1 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-51)
51655-474-52 51655-474 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210114 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-474-52)
80425-0089-1 80425-0089 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0089-1)
80425-0089-2 80425-0089 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20151230 N/A ANDA ANDA090796 Advanced Rx of Tennessee, LLC IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (80425-0089-2)
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