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=ANDA078341"
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
70518-1704-1 70518-1704 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20240219 N/A ANDA ANDA078341 REMEDYREPACK INC. FINASTERIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1704-1)
76420-154-30 76420-154 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20210728 N/A ANDA ANDA078341 Asclemed USA, Inc. FINASTERIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-154-30)
76420-154-90 76420-154 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20210728 N/A ANDA ANDA078341 Asclemed USA, Inc. FINASTERIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-154-90)
82009-061-05 82009-061 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20221121 N/A ANDA ANDA078341 QUALLENT PHARMACEUTICALS HEALTH LLC FINASTERIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (82009-061-05)
68071-3417-3 68071-3417 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20230526 N/A ANDA ANDA078341 NuCare Pharmaceuticals,Inc. FINASTERIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3417-3)
50090-6941-0 50090-6941 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20231215 N/A ANDA ANDA078341 A-S Medication Solutions FINASTERIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6941-0)
71335-1530-1 71335-1530 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20211228 N/A ANDA ANDA078341 Bryant Ranch Prepack FINASTERIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-1530-1)
71335-1530-2 71335-1530 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20200306 N/A ANDA ANDA078341 Bryant Ranch Prepack FINASTERIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1530-2)
71335-1530-3 71335-1530 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20211228 N/A ANDA ANDA078341 Bryant Ranch Prepack FINASTERIDE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1530-3)
71335-1530-4 71335-1530 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20200320 N/A ANDA ANDA078341 Bryant Ranch Prepack FINASTERIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1530-4)
71335-1530-5 71335-1530 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20211228 N/A ANDA ANDA078341 Bryant Ranch Prepack FINASTERIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (71335-1530-5)
71335-1530-6 71335-1530 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20211228 N/A ANDA ANDA078341 Bryant Ranch Prepack FINASTERIDE 5 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71335-1530-6)
70518-3616-3 70518-3616 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA078341 REMEDYREPACK INC. FINASTERIDE 5 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3616-3)
70518-3616-4 70518-3616 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20240125 N/A ANDA ANDA078341 REMEDYREPACK INC. FINASTERIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3616-4)
70518-3616-5 70518-3616 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20240807 N/A ANDA ANDA078341 REMEDYREPACK INC. FINASTERIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3616-5)
50090-6940-0 50090-6940 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20231215 N/A ANDA ANDA078341 A-S Medication Solutions FINASTERIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-6940-0)
50090-6940-1 50090-6940 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20231215 N/A ANDA ANDA078341 A-S Medication Solutions FINASTERIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6940-1)
50090-6940-2 50090-6940 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20231215 N/A ANDA ANDA078341 A-S Medication Solutions FINASTERIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (50090-6940-2)
68071-1648-9 68071-1648 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20170609 N/A ANDA ANDA078341 NuCare Pharmaceuticals, Inc. FINASTERIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-1648-9)
65862-149-01 65862-149 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20071030 N/A ANDA ANDA078341 Aurobindo Pharma Limited FINASTERIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-149-01)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase