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=ANDA091448"
符合检索条件的记录共 45 条，共 3 页，当前第 2 页 ，可点击列名称排序
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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
71335-3111-6 71335-3111 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL TABLET, FILM COATED ORAL 20260330 N/A ANDA ANDA091448 Bryant Ranch Prepack SILDENAFIL CITRATE 50 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-3111-6)
71335-3111-7 71335-3111 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL TABLET, FILM COATED ORAL 20260330 N/A ANDA ANDA091448 Bryant Ranch Prepack SILDENAFIL CITRATE 50 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (71335-3111-7)
71335-3111-8 71335-3111 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL TABLET, FILM COATED ORAL 20260330 N/A ANDA ANDA091448 Bryant Ranch Prepack SILDENAFIL CITRATE 50 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71335-3111-8)
68071-3862-5 68071-3862 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL TABLET, FILM COATED ORAL 20250611 N/A ANDA ANDA091448 NuCare Pharmaceuticals, Inc. SILDENAFIL CITRATE 100 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68071-3862-5)
68071-3862-6 68071-3862 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL TABLET, FILM COATED ORAL 20250611 N/A ANDA ANDA091448 NuCare Pharmaceuticals, Inc. SILDENAFIL CITRATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-3862-6)
68071-3862-9 68071-3862 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL TABLET, FILM COATED ORAL 20250605 N/A ANDA ANDA091448 NuCare Pharmaceuticals, Inc. SILDENAFIL CITRATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-3862-9)
71205-231-10 71205-231 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20190301 N/A ANDA ANDA091448 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71205-231-10)
71205-231-20 71205-231 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20231019 N/A ANDA ANDA091448 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71205-231-20)
71205-231-30 71205-231 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20190301 N/A ANDA ANDA091448 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-231-30)
71205-231-60 71205-231 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20190301 N/A ANDA ANDA091448 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-231-60)
71205-231-90 71205-231 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20190301 N/A ANDA ANDA091448 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-231-90)
13668-188-01 13668-188 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL TABLET, FILM COATED ORAL 20180611 N/A ANDA ANDA091448 Torrent Pharmaceuticals Limited SILDENAFIL CITRATE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (13668-188-01)
13668-188-05 13668-188 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL TABLET, FILM COATED ORAL 20180611 N/A ANDA ANDA091448 Torrent Pharmaceuticals Limited SILDENAFIL CITRATE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (13668-188-05)
13668-188-10 13668-188 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL TABLET, FILM COATED ORAL 20180611 N/A ANDA ANDA091448 Torrent Pharmaceuticals Limited SILDENAFIL CITRATE 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (13668-188-10)
13668-188-30 13668-188 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL TABLET, FILM COATED ORAL 20180611 N/A ANDA ANDA091448 Torrent Pharmaceuticals Limited SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (13668-188-30)
43063-941-15 43063-941 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL TABLET, FILM COATED ORAL 20190130 N/A ANDA ANDA091448 PD-Rx Pharmaceuticals, Inc. SILDENAFIL CITRATE 50 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-941-15)
51655-794-54 51655-794 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL TABLET, FILM COATED ORAL 20220120 N/A ANDA ANDA091448 Northwind Health Company, LLC SILDENAFIL CITRATE 100 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-794-54)
51655-794-87 51655-794 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL TABLET, FILM COATED ORAL 20220120 N/A ANDA ANDA091448 Northwind Health Company, LLC SILDENAFIL CITRATE 100 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-794-87)
13668-187-01 13668-187 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL TABLET, FILM COATED ORAL 20180611 N/A ANDA ANDA091448 Torrent Pharmaceuticals Limited SILDENAFIL CITRATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (13668-187-01)
13668-187-05 13668-187 HUMAN PRESCRIPTION DRUG SILDENAFIL CITRATE SILDENAFIL TABLET, FILM COATED ORAL 20180611 N/A ANDA ANDA091448 Torrent Pharmaceuticals Limited SILDENAFIL CITRATE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (13668-187-05)
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