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=ANDA208960"
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
70710-1068-1 70710-1068 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA208960 Zydus Pharmaceuticals USA Inc. VARDENAFIL HYDROCHLORIDE TRIHYDRATE 2.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1068-1)
70710-1068-3 70710-1068 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA208960 Zydus Pharmaceuticals USA Inc. VARDENAFIL HYDROCHLORIDE TRIHYDRATE 2.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70710-1068-3)
70710-1068-9 70710-1068 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA208960 Zydus Pharmaceuticals USA Inc. VARDENAFIL HYDROCHLORIDE TRIHYDRATE 2.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70710-1068-9)
70771-1049-1 70771-1049 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA208960 Zydus Lifesciences Limited VARDENAFIL HYDROCHLORIDE TRIHYDRATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1049-1)
70771-1049-3 70771-1049 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA208960 Zydus Lifesciences Limited VARDENAFIL HYDROCHLORIDE TRIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70771-1049-3)
70771-1049-9 70771-1049 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA208960 Zydus Lifesciences Limited VARDENAFIL HYDROCHLORIDE TRIHYDRATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70771-1049-9)
70710-1070-1 70710-1070 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA208960 Zydus Pharmaceuticals USA Inc. VARDENAFIL HYDROCHLORIDE TRIHYDRATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1070-1)
70710-1070-3 70710-1070 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA208960 Zydus Pharmaceuticals USA Inc. VARDENAFIL HYDROCHLORIDE TRIHYDRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70710-1070-3)
70710-1070-9 70710-1070 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA208960 Zydus Pharmaceuticals USA Inc. VARDENAFIL HYDROCHLORIDE TRIHYDRATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70710-1070-9)
70771-1047-1 70771-1047 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA208960 Zydus Lifesciences Limited VARDENAFIL HYDROCHLORIDE TRIHYDRATE 2.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1047-1)
70771-1047-3 70771-1047 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA208960 Zydus Lifesciences Limited VARDENAFIL HYDROCHLORIDE TRIHYDRATE 2.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70771-1047-3)
70771-1047-9 70771-1047 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA208960 Zydus Lifesciences Limited VARDENAFIL HYDROCHLORIDE TRIHYDRATE 2.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70771-1047-9)
70710-1071-1 70710-1071 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA208960 Zydus Pharmaceuticals USA Inc. VARDENAFIL HYDROCHLORIDE TRIHYDRATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1071-1)
70710-1071-3 70710-1071 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA208960 Zydus Pharmaceuticals USA Inc. VARDENAFIL HYDROCHLORIDE TRIHYDRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70710-1071-3)
70710-1071-9 70710-1071 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA208960 Zydus Pharmaceuticals USA Inc. VARDENAFIL HYDROCHLORIDE TRIHYDRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70710-1071-9)
71610-643-02 71610-643 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20220421 N/A ANDA ANDA208960 Aphena Pharma Solutions - Tennessee, LLC VARDENAFIL HYDROCHLORIDE TRIHYDRATE 20 mg/1 2 TABLET, FILM COATED in 1 BOTTLE (71610-643-02)
71610-643-04 71610-643 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20220421 N/A ANDA ANDA208960 Aphena Pharma Solutions - Tennessee, LLC VARDENAFIL HYDROCHLORIDE TRIHYDRATE 20 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (71610-643-04)
71610-643-06 71610-643 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20220421 N/A ANDA ANDA208960 Aphena Pharma Solutions - Tennessee, LLC VARDENAFIL HYDROCHLORIDE TRIHYDRATE 20 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (71610-643-06)
71610-643-12 71610-643 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20220421 N/A ANDA ANDA208960 Aphena Pharma Solutions - Tennessee, LLC VARDENAFIL HYDROCHLORIDE TRIHYDRATE 20 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (71610-643-12)
70771-1048-1 70771-1048 HUMAN PRESCRIPTION DRUG VARDENAFIL VARDENAFIL TABLET, FILM COATED ORAL 20181101 N/A ANDA ANDA208960 Zydus Lifesciences Limited VARDENAFIL HYDROCHLORIDE TRIHYDRATE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1048-1)
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