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
29300-286-01 29300-286 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209250 Unichem Pharmaceuticals (USA), Inc. TADALAFIL 2.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-286-01)
29300-286-05 29300-286 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209250 Unichem Pharmaceuticals (USA), Inc. TADALAFIL 2.5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-286-05)
29300-286-13 29300-286 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209250 Unichem Pharmaceuticals (USA), Inc. TADALAFIL 2.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-286-13)
29300-286-82 29300-286 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209250 Unichem Pharmaceuticals (USA), Inc. TADALAFIL 2.5 mg/1 2 BLISTER PACK in 1 CARTON (29300-286-82) / 15 TABLET, FILM COATED in 1 BLISTER PACK (29300-286-51)
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