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=ANDA077342"
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
0093-5343-56 0093-5343 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20171211 N/A ANDA ANDA077342 Teva Pharmaceuticals USA, Inc. SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0093-5343-56)
71610-237-02 71610-237 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190208 N/A ANDA ANDA077342 Aphena Pharma Solutions - Tennessee, LLC SILDENAFIL CITRATE 100 mg/1 2 TABLET, FILM COATED in 1 BOTTLE (71610-237-02)
71610-237-03 71610-237 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20221004 N/A ANDA ANDA077342 Aphena Pharma Solutions - Tennessee, LLC SILDENAFIL CITRATE 100 mg/1 9 TABLET, FILM COATED in 1 BOTTLE (71610-237-03)
71610-237-04 71610-237 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190208 N/A ANDA ANDA077342 Aphena Pharma Solutions - Tennessee, LLC SILDENAFIL CITRATE 100 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (71610-237-04)
71205-267-20 71205-267 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190501 N/A ANDA ANDA077342 Proficient Rx LP SILDENAFIL CITRATE 50 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71205-267-20)
71205-267-30 71205-267 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190501 N/A ANDA ANDA077342 Proficient Rx LP SILDENAFIL CITRATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-267-30)
71205-267-60 71205-267 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190501 N/A ANDA ANDA077342 Proficient Rx LP SILDENAFIL CITRATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-267-60)
71205-267-90 71205-267 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190501 N/A ANDA ANDA077342 Proficient Rx LP SILDENAFIL CITRATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-267-90)
0093-5342-01 0093-5342 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20171211 N/A ANDA ANDA077342 Teva Pharmaceuticals USA, Inc. SILDENAFIL CITRATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0093-5342-01)
0093-5342-56 0093-5342 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20171211 N/A ANDA ANDA077342 Teva Pharmaceuticals USA, Inc. SILDENAFIL CITRATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0093-5342-56)
71205-088-10 71205-088 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180801 N/A ANDA ANDA077342 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71205-088-10)
71205-088-20 71205-088 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20210421 N/A ANDA ANDA077342 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71205-088-20)
71205-088-30 71205-088 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180801 N/A ANDA ANDA077342 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-088-30)
71205-088-50 71205-088 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180801 N/A ANDA ANDA077342 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (71205-088-50)
71205-088-60 71205-088 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180801 N/A ANDA ANDA077342 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-088-60)
71205-088-90 71205-088 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180801 N/A ANDA ANDA077342 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-088-90)
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