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"
符合检索条件的记录共 147 条，共 8 页，当前第 4 页 ，可点击列名称排序
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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
68071-3362-5 68071-3362 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68071-3362-5)
68071-3362-6 68071-3362 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-3362-6)
68071-3362-9 68071-3362 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170726 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-3362-9)
42708-097-30 42708-097 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20190531 N/A ANDA ANDA090796 QPharma, Inc. IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (42708-097-30)
51655-275-20 51655-275 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210709 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 800 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-20)
51655-275-21 51655-275 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20201029 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 800 mg/1 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-21)
51655-275-25 51655-275 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210217 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-25)
51655-275-26 51655-275 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20200616 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-26)
51655-275-54 51655-275 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20200921 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 800 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-54)
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)
51655-759-52 51655-759 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210805 N/A ANDA ANDA090796 Northwind Health Company, LLC IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-759-52)
68071-4009-1 68071-4009 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170719 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (68071-4009-1)
68071-4009-2 68071-4009 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170719 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68071-4009-2)
68071-4009-3 68071-4009 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170719 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-4009-3)
68071-4009-4 68071-4009 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170719 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (68071-4009-4)
68071-4009-5 68071-4009 HUMAN PRESCRIPTION DRUG IBUPROFEN IBUPROFEN TABLET, FILM COATED ORAL 20170719 N/A ANDA ANDA090796 NuCare Pharmaceuticals,Inc. IBUPROFEN 600 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (68071-4009-5)
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