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=ANDA217400"
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
71335-2805-8 71335-2805 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20251014 N/A ANDA ANDA217400 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (71335-2805-8)
71335-2805-9 71335-2805 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20251014 N/A ANDA ANDA217400 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71335-2805-9)
67296-2186-3 67296-2186 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20240918 N/A ANDA ANDA217400 Redpharm Drug FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (67296-2186-3)
68788-4021-3 68788-4021 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20250905 N/A ANDA ANDA217400 Preferred Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-4021-3)
68788-4021-4 68788-4021 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20250905 N/A ANDA ANDA217400 Preferred Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (68788-4021-4)
68788-4021-6 68788-4021 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20250905 N/A ANDA ANDA217400 Preferred Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-4021-6)
68788-4021-9 68788-4021 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20250905 N/A ANDA ANDA217400 Preferred Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-4021-9)
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