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=ANDA203814"
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
63187-813-90 63187-813 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA203814 Proficient Rx LP SILDENAFIL CITRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-813-90)
76420-061-30 76420-061 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20191210 N/A ANDA ANDA203814 Asclemed USA, Inc. SILDENAFIL CITRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-061-30)
76420-061-60 76420-061 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20220831 N/A ANDA ANDA203814 Asclemed USA, Inc. SILDENAFIL CITRATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-061-60)
76420-061-90 76420-061 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20191210 N/A ANDA ANDA203814 Asclemed USA, Inc. SILDENAFIL CITRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-061-90)
68001-363-05 68001-363 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180914 20271031 ANDA ANDA203814 BluePoint Laboratories SILDENAFIL CITRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68001-363-05)
68071-5115-6 68071-5115 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20140103 20271031 ANDA ANDA203814 NuCare Pharmaceuticals,Inc. SILDENAFIL CITRATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-5115-6)
71335-1638-1 71335-1638 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20140103 N/A ANDA ANDA203814 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71335-1638-1)
71335-1638-2 71335-1638 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20140103 N/A ANDA ANDA203814 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1638-2)
71335-1638-3 71335-1638 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20140103 N/A ANDA ANDA203814 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (71335-1638-3)
71335-1638-4 71335-1638 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20140103 N/A ANDA ANDA203814 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1638-4)
71335-1638-5 71335-1638 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20140103 N/A ANDA ANDA203814 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1638-5)
71335-1638-6 71335-1638 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20140103 N/A ANDA ANDA203814 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-1638-6)
71335-1638-7 71335-1638 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20140103 N/A ANDA ANDA203814 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 270 TABLET, FILM COATED in 1 BOTTLE (71335-1638-7)
71335-1638-8 71335-1638 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20140103 N/A ANDA ANDA203814 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-1638-8)
71335-1638-9 71335-1638 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20140103 N/A ANDA ANDA203814 Bryant Ranch Prepack SILDENAFIL CITRATE 20 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (71335-1638-9)
68071-4517-9 68071-4517 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180803 20271031 ANDA ANDA203814 NuCare Pharmaceuticals,Inc. SILDENAFIL CITRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-4517-9)
60687-788-21 60687-788 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20231113 N/A ANDA ANDA203814 American Health Packaging SILDENAFIL CITRATE 20 mg/1 30 BLISTER PACK in 1 CARTON (60687-788-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-788-11)
33342-536-10 33342-536 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20140103 N/A ANDA ANDA203814 Macleods Pharmaceuticals Limited SILDENAFIL CITRATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (33342-536-10)
33342-536-58 33342-536 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20220113 N/A ANDA ANDA203814 Macleods Pharmaceuticals Limited SILDENAFIL CITRATE 20 mg/1 6500 TABLET, FILM COATED in 1 POUCH (33342-536-58)
33342-536-66 33342-536 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20140103 N/A ANDA ANDA203814 Macleods Pharmaceuticals Limited SILDENAFIL CITRATE 20 mg/1 10 TABLET, FILM COATED in 1 BLISTER PACK (33342-536-66)
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