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
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)
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)
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