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
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)
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)
57237-062-05 57237-062 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20071030 N/A ANDA ANDA078341 Rising Pharma Holdings, Inc. FINASTERIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (57237-062-05)
57237-062-30 57237-062 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20071030 N/A ANDA ANDA078341 Rising Pharma Holdings, Inc. FINASTERIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (57237-062-30)
57237-062-90 57237-062 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20071030 N/A ANDA ANDA078341 Rising Pharma Holdings, Inc. FINASTERIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (57237-062-90)
68071-3234-9 68071-3234 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20180122 N/A ANDA ANDA078341 NuCare Pharmaceuticals,Inc. FINASTERIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-3234-9)
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)
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)
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)
65862-149-05 65862-149 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20071030 N/A ANDA ANDA078341 Aurobindo Pharma Limited FINASTERIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-149-05)
65862-149-30 65862-149 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20071030 N/A ANDA ANDA078341 Aurobindo Pharma Limited FINASTERIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-149-30)
65862-149-90 65862-149 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20071030 N/A ANDA ANDA078341 Aurobindo Pharma Limited FINASTERIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-149-90)
68071-3785-2 68071-3785 HUMAN PRESCRIPTION DRUG Finasteride Finasteride TABLET, FILM COATED ORAL 20250123 N/A ANDA ANDA078341 NuCare Pharmaceuticals, Inc. FINASTERIDE 5 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (68071-3785-2)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase