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=ANDA208709"
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
50090-5327-0 50090-5327 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20201030 N/A ANDA ANDA208709 A-S Medication Solutions FENOFIBRATE 48 mg/1 90 TABLET in 1 BOTTLE (50090-5327-0)
68071-5101-9 68071-5101 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20191104 N/A ANDA ANDA208709 NuCare Pharmaceuticals,Inc. FENOFIBRATE 145 mg/1 90 TABLET in 1 BOTTLE (68071-5101-9)
69097-458-02 69097-458 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20161215 N/A ANDA ANDA208709 Cipla USA Inc. FENOFIBRATE 145 mg/1 30 TABLET in 1 BOTTLE (69097-458-02)
69097-458-05 69097-458 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20161215 N/A ANDA ANDA208709 Cipla USA Inc. FENOFIBRATE 145 mg/1 90 TABLET in 1 BOTTLE (69097-458-05)
71335-0891-1 71335-0891 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20210408 N/A ANDA ANDA208709 Bryant Ranch Prepack FENOFIBRATE 48 mg/1 30 TABLET in 1 BOTTLE (71335-0891-1)
71335-0891-2 71335-0891 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20180702 N/A ANDA ANDA208709 Bryant Ranch Prepack FENOFIBRATE 48 mg/1 90 TABLET in 1 BOTTLE (71335-0891-2)
71335-0891-3 71335-0891 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20211227 N/A ANDA ANDA208709 Bryant Ranch Prepack FENOFIBRATE 48 mg/1 28 TABLET in 1 BOTTLE (71335-0891-3)
69097-459-02 69097-459 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20161215 N/A ANDA ANDA208709 Cipla USA Inc. FENOFIBRATE 48 mg/1 30 TABLET in 1 BOTTLE (69097-459-02)
69097-459-05 69097-459 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20161215 N/A ANDA ANDA208709 Cipla USA Inc. FENOFIBRATE 48 mg/1 90 TABLET in 1 BOTTLE (69097-459-05)
51655-234-52 51655-234 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20220816 N/A ANDA ANDA208709 Northwind Pharmaceuticals, LLC FENOFIBRATE 145 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-234-52)
51655-866-52 51655-866 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20230710 N/A ANDA ANDA208709 Northwind Pharmaceuticals, LLC FENOFIBRATE 48 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-866-52)
0615-8530-39 0615-8530 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20240918 N/A ANDA ANDA208709 NCS HealthCare of KY, LLC dba Vangard Labs FENOFIBRATE 145 mg/1 30 TABLET in 1 BLISTER PACK (0615-8530-39)
0904-7161-04 0904-7161 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20161215 N/A ANDA ANDA208709 Major Pharmaceuticals FENOFIBRATE 145 mg/1 30 BLISTER PACK in 1 CARTON (0904-7161-04) / 1 TABLET in 1 BLISTER PACK
0904-7161-61 0904-7161 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20161215 N/A ANDA ANDA208709 Major Pharmaceuticals FENOFIBRATE 145 mg/1 100 BLISTER PACK in 1 CARTON (0904-7161-61) / 1 TABLET in 1 BLISTER PACK
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