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=ANDA076509"
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
50090-6973-0 50090-6973 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20231221 N/A ANDA ANDA076509 A-S Medication Solutions FENOFIBRATE 160 mg/1 30 TABLET in 1 BOTTLE (50090-6973-0)
50090-6973-1 50090-6973 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20231221 N/A ANDA ANDA076509 A-S Medication Solutions FENOFIBRATE 160 mg/1 90 TABLET in 1 BOTTLE (50090-6973-1)
50090-6974-0 50090-6974 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20231221 N/A ANDA ANDA076509 A-S Medication Solutions FENOFIBRATE 160 mg/1 90 TABLET in 1 BOTTLE (50090-6974-0)
0115-5511-01 0115-5511 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20100201 N/A ANDA ANDA076509 Amneal Pharmaceuticals of New York LLC FENOFIBRATE 54 mg/1 100 TABLET in 1 BOTTLE (0115-5511-01)
0115-5511-02 0115-5511 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20100201 N/A ANDA ANDA076509 Amneal Pharmaceuticals of New York LLC FENOFIBRATE 54 mg/1 500 TABLET in 1 BOTTLE (0115-5511-02)
0115-5511-03 0115-5511 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20100201 N/A ANDA ANDA076509 Amneal Pharmaceuticals of New York LLC FENOFIBRATE 54 mg/1 1000 TABLET in 1 BOTTLE (0115-5511-03)
0115-5511-10 0115-5511 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20100201 N/A ANDA ANDA076509 Amneal Pharmaceuticals of New York LLC FENOFIBRATE 54 mg/1 90 TABLET in 1 BOTTLE (0115-5511-10)
0115-5522-01 0115-5522 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20100201 N/A ANDA ANDA076509 Amneal Pharmaceuticals of New York LLC FENOFIBRATE 160 mg/1 100 TABLET in 1 BOTTLE (0115-5522-01)
0115-5522-02 0115-5522 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20100201 N/A ANDA ANDA076509 Amneal Pharmaceuticals of New York LLC FENOFIBRATE 160 mg/1 500 TABLET in 1 BOTTLE (0115-5522-02)
0115-5522-03 0115-5522 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20100201 N/A ANDA ANDA076509 Amneal Pharmaceuticals of New York LLC FENOFIBRATE 160 mg/1 1000 TABLET in 1 BOTTLE (0115-5522-03)
0115-5522-10 0115-5522 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20100201 N/A ANDA ANDA076509 Amneal Pharmaceuticals of New York LLC FENOFIBRATE 160 mg/1 90 TABLET in 1 BOTTLE (0115-5522-10)
50268-312-15 50268-312 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20150813 N/A ANDA ANDA076509 AvPAK FENOFIBRATE 54 mg/1 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-312-15) / 1 TABLET in 1 BLISTER PACK (50268-312-11)
50268-313-15 50268-313 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20150813 N/A ANDA ANDA076509 AvPAK FENOFIBRATE 160 mg/1 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-313-15) / 1 TABLET in 1 BLISTER PACK (50268-313-11)
51655-009-52 51655-009 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20140507 N/A ANDA ANDA076509 Northwind Pharmaceuticals FENOFIBRATE 160 mg/1 30 TABLET in 1 BOTTLE, DISPENSING (51655-009-52)
60219-5511-9 60219-5511 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20220622 N/A ANDA ANDA076509 Amneal Pharmaceuticals NY LLC FENOFIBRATE 54 mg/1 90 TABLET in 1 BOTTLE (60219-5511-9)
60219-5522-5 60219-5522 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20220622 N/A ANDA ANDA076509 Amneal Pharmaceuticals NY LLC FENOFIBRATE 160 mg/1 500 TABLET in 1 BOTTLE (60219-5522-5)
60219-5522-9 60219-5522 HUMAN PRESCRIPTION DRUG FENOFIBRATE FENOFIBRATE TABLET ORAL 20220622 N/A ANDA ANDA076509 Amneal Pharmaceuticals NY LLC FENOFIBRATE 160 mg/1 90 TABLET in 1 BOTTLE (60219-5522-9)
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