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=NDA017955"
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
0378-8085-15 0378-8085 HUMAN PRESCRIPTION DRUG Tretinoin Tretinoin GEL TOPICAL 20190812 N/A NDA AUTHORIZED GENERIC NDA017955 Mylan Pharmaceuticals Inc. TRETINOIN .1 mg/g 1 TUBE in 1 CARTON (0378-8085-15) / 15 g in 1 TUBE
0378-8085-45 0378-8085 HUMAN PRESCRIPTION DRUG Tretinoin Tretinoin GEL TOPICAL 20190812 N/A NDA AUTHORIZED GENERIC NDA017955 Mylan Pharmaceuticals Inc. TRETINOIN .1 mg/g 1 TUBE in 1 CARTON (0378-8085-45) / 45 g in 1 TUBE
63629-9123-1 63629-9123 HUMAN PRESCRIPTION DRUG Tretinoin Tretinoin GEL TOPICAL 20230216 N/A NDA AUTHORIZED GENERIC NDA017955 Bryant Ranch Prepack TRETINOIN .1 mg/g 1 TUBE in 1 CARTON (63629-9123-1) / 45 g in 1 TUBE
0187-5172-15 0187-5172 HUMAN PRESCRIPTION DRUG Retin-A Tretinoin GEL TOPICAL 19790730 N/A NDA NDA017955 Bausch Health US, LLC TRETINOIN .1 mg/g 1 TUBE in 1 CARTON (0187-5172-15) / 15 g in 1 TUBE
0187-5172-45 0187-5172 HUMAN PRESCRIPTION DRUG Retin-A Tretinoin GEL TOPICAL 19790730 N/A NDA NDA017955 Bausch Health US, LLC TRETINOIN .1 mg/g 1 TUBE in 1 CARTON (0187-5172-45) / 45 g in 1 TUBE
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