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=ANDA209250"
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
68071-3586-9 68071-3586 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20240314 N/A ANDA ANDA209250 NuCare Pharmaceuticals,Inc. TADALAFIL 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3586-9)
68071-3777-4 68071-3777 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250120 N/A ANDA ANDA209250 NuCare Pharmaceuticals,Inc. TADALAFIL 20 mg/1 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3777-4)
68071-3777-5 68071-3777 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250120 N/A ANDA ANDA209250 NuCare Pharmaceuticals,Inc. TADALAFIL 20 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3777-5)
68071-3777-6 68071-3777 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250421 N/A ANDA ANDA209250 NuCare Pharmaceuticals,Inc. TADALAFIL 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3777-6)
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