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=ANDA091479"
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
13668-185-51 13668-185 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20121106 N/A ANDA ANDA091479 Torrent Pharmaceuticals Limited SILDENAFIL CITRATE 20 mg/1 5000 TABLET, FILM COATED in 1 BOTTLE (13668-185-51)
13668-185-90 13668-185 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20121106 N/A ANDA ANDA091479 Torrent Pharmaceuticals Limited SILDENAFIL CITRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (13668-185-90)
13668-185-30 13668-185 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20121106 N/A ANDA ANDA091479 Torrent Pharmaceuticals Limited SILDENAFIL CITRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (13668-185-30)
71335-2657-0 71335-2657 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20250623 N/A ANDA ANDA091479 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (71335-2657-0)
13668-185-10 13668-185 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20241204 N/A ANDA ANDA091479 Torrent Pharmaceuticals Limited SILDENAFIL CITRATE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (13668-185-10)
13668-185-05 13668-185 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20121106 N/A ANDA ANDA091479 Torrent Pharmaceuticals Limited SILDENAFIL CITRATE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (13668-185-05)
68071-3954-9 68071-3954 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20260119 N/A ANDA ANDA091479 NuCare Pharmaceuticals, Inc. SILDENAFIL CITRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-3954-9)
71335-2657-4 71335-2657 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20250623 N/A ANDA ANDA091479 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-2657-4)
71335-2657-5 71335-2657 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20250623 N/A ANDA ANDA091479 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-2657-5)
71335-2657-6 71335-2657 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20250623 N/A ANDA ANDA091479 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-2657-6)
71335-2657-7 71335-2657 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20250623 N/A ANDA ANDA091479 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 270 TABLET, FILM COATED in 1 BOTTLE (71335-2657-7)
71335-2657-8 71335-2657 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20250623 N/A ANDA ANDA091479 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-2657-8)
71335-2657-9 71335-2657 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20250623 N/A ANDA ANDA091479 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (71335-2657-9)
71335-2657-1 71335-2657 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20250623 N/A ANDA ANDA091479 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71335-2657-1)
71335-2657-2 71335-2657 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20250623 N/A ANDA ANDA091479 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2657-2)
71335-2657-3 71335-2657 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20250623 N/A ANDA ANDA091479 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (71335-2657-3)
76420-613-30 76420-613 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL CITRATE TABLET ORAL 20230913 N/A ANDA ANDA091479 Asclemed USA, Inc. SILDENAFIL CITRATE 20 mg/1 30 TABLET in 1 BOTTLE (76420-613-30)
76420-613-60 76420-613 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL CITRATE TABLET ORAL 20230913 N/A ANDA ANDA091479 Asclemed USA, Inc. SILDENAFIL CITRATE 20 mg/1 60 TABLET in 1 BOTTLE (76420-613-60)
55154-4307-0 55154-4307 HUMAN PRESCRIPTION DRUG SILDENAFIL SILDENAFIL TABLET, FILM COATED ORAL 20121106 N/A ANDA ANDA091479 Cardinal Health 107, LLC SILDENAFIL CITRATE 20 mg/1 10 BLISTER PACK in 1 BAG (55154-4307-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
76420-613-90 76420-613 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL CITRATE TABLET ORAL 20230913 N/A ANDA ANDA091479 Asclemed USA, Inc. SILDENAFIL CITRATE 20 mg/1 90 TABLET in 1 BOTTLE (76420-613-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase