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=ANDA091625"
符合检索条件的记录共 254 条，共 13 页，当前第 7 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
70518-1364-2 70518-1364 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20201023 N/A ANDA ANDA091625 REMEDYREPACK INC. IBUPROFEN 600 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1364-2)
70518-1364-4 70518-1364 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230730 N/A ANDA ANDA091625 REMEDYREPACK INC. IBUPROFEN 600 mg/1 27 TABLET, FILM COATED in 1 BLISTER PACK (70518-1364-4)
70518-1364-8 70518-1364 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251205 N/A ANDA ANDA091625 REMEDYREPACK INC. IBUPROFEN 600 mg/1 100 POUCH in 1 BOX (70518-1364-8) / 1 TABLET, FILM COATED in 1 POUCH (70518-1364-9)
50090-6645-0 50090-6645 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230829 N/A ANDA ANDA091625 A-S Medication Solutions IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6645-0)
51655-042-20 51655-042 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230108 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 600 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-042-20)
51655-042-25 51655-042 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220909 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-042-25)
51655-042-26 51655-042 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20221214 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-042-26)
51655-385-20 51655-385 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230220 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 800 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-20)
51655-385-21 51655-385 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20200521 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 800 mg/1 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-21)
51655-385-25 51655-385 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230407 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-25)
51655-385-26 51655-385 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220908 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-26)
51655-385-51 51655-385 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20200521 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 800 mg/1 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-51)
51655-385-52 51655-385 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20200521 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-52)
51655-385-54 51655-385 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210507 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 800 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-385-54)
51655-042-52 51655-042 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20230628 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-042-52)
51655-048-26 51655-048 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20200520 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-048-26)
51655-048-52 51655-048 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20221014 N/A ANDA ANDA091625 Northwind Health Company, LLC IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-048-52)
54348-825-08 54348-825 HUMAN PRESCRIPTION DRUG Ibuprofen IBUPROFEN TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA091625 PharmPak, Inc. IBUPROFEN 800 mg/1 1 BOTTLE in 1 BOX (54348-825-08) / 8 TABLET, FILM COATED in 1 BOTTLE
54348-825-10 54348-825 HUMAN PRESCRIPTION DRUG Ibuprofen IBUPROFEN TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA091625 PharmPak, Inc. IBUPROFEN 800 mg/1 1 BOTTLE in 1 BOX (54348-825-10) / 10 TABLET, FILM COATED in 1 BOTTLE
54348-825-12 54348-825 HUMAN PRESCRIPTION DRUG Ibuprofen IBUPROFEN TABLET, FILM COATED ORAL 20190711 N/A ANDA ANDA091625 PharmPak, Inc. IBUPROFEN 800 mg/1 1 BOTTLE in 1 BOX (54348-825-12) / 12 TABLET, FILM COATED in 1 BOTTLE
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