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=ANDA209167"
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
16729-370-16 16729-370 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20200427 N/A ANDA ANDA209167 Accord Healthcare Inc. TADALAFIL 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (16729-370-16)
16729-371-10 16729-371 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20200403 N/A ANDA ANDA209167 Accord Healthcare Inc. TADALAFIL 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16729-371-10)
16729-371-16 16729-371 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20200429 N/A ANDA ANDA209167 Accord Healthcare Inc. TADALAFIL 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (16729-371-16)
16729-372-10 16729-372 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190327 N/A ANDA ANDA209167 Accord Healthcare Inc. TADALAFIL 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16729-372-10)
16729-372-16 16729-372 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20200429 N/A ANDA ANDA209167 Accord Healthcare Inc. TADALAFIL 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (16729-372-16)
76420-126-15 76420-126 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20220129 N/A ANDA ANDA209167 Asclemed USA, Inc. TADALAFIL 5 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (76420-126-15)
76420-126-30 76420-126 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20200730 N/A ANDA ANDA209167 Asclemed USA, Inc. TADALAFIL 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-126-30)
76420-126-90 76420-126 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20200730 N/A ANDA ANDA209167 Asclemed USA, Inc. TADALAFIL 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-126-90)
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