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=ANDA203962"
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
71205-220-50 71205-220 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA203962 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (71205-220-50)
71205-220-60 71205-220 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA203962 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-220-60)
71205-220-90 71205-220 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA203962 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-220-90)
71205-220-30 71205-220 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA203962 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-220-30)
71205-220-20 71205-220 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA203962 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71205-220-20)
71205-220-10 71205-220 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA203962 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71205-220-10)
68071-3832-3 68071-3832 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20250418 N/A ANDA ANDA203962 NuCare Pharmaceuticals, Inc. SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3832-3)
68071-3908-1 68071-3908 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20251021 N/A ANDA ANDA203962 NuCare Pharmaceuticals,Inc. SILDENAFIL CITRATE 100 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (68071-3908-1)
68071-3743-3 68071-3743 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20241210 N/A ANDA ANDA203962 NuCare Pharmaceuticals, Inc. SILDENAFIL CITRATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3743-3)
68071-3745-5 68071-3745 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20251009 N/A ANDA ANDA203962 NuCare Pharmaceuticals, Inc. SILDENAFIL CITRATE 50 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (68071-3745-5)
68071-3745-6 68071-3745 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20241212 N/A ANDA ANDA203962 NuCare Pharmaceuticals, Inc. SILDENAFIL CITRATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-3745-6)
65862-689-05 65862-689 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20230710 N/A ANDA ANDA203962 Aurobindo Pharma Limited SILDENAFIL CITRATE 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-689-05)
65862-690-01 65862-690 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180611 N/A ANDA ANDA203962 Aurobindo Pharma Limited SILDENAFIL CITRATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-690-01)
65862-690-05 65862-690 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20230710 N/A ANDA ANDA203962 Aurobindo Pharma Limited SILDENAFIL CITRATE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-690-05)
65862-690-30 65862-690 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180611 N/A ANDA ANDA203962 Aurobindo Pharma Limited SILDENAFIL CITRATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-690-30)
65862-690-99 65862-690 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180611 N/A ANDA ANDA203962 Aurobindo Pharma Limited SILDENAFIL CITRATE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-690-99)
65862-691-01 65862-691 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180611 N/A ANDA ANDA203962 Aurobindo Pharma Limited SILDENAFIL CITRATE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-691-01)
65862-691-05 65862-691 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180611 N/A ANDA ANDA203962 Aurobindo Pharma Limited SILDENAFIL CITRATE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-691-05)
65862-691-30 65862-691 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180611 N/A ANDA ANDA203962 Aurobindo Pharma Limited SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-691-30)
65862-689-30 65862-689 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180611 N/A ANDA ANDA203962 Aurobindo Pharma Limited SILDENAFIL CITRATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-689-30)
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