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=ANDA075718"
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
82804-194-10 82804-194 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20250528 N/A ANDA ANDA075718 Proficient Rx LP FAMOTIDINE 20 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (82804-194-10)
82804-194-30 82804-194 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20250425 N/A ANDA ANDA075718 Proficient Rx LP FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (82804-194-30)
82804-194-78 82804-194 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20250605 N/A ANDA ANDA075718 Proficient Rx LP FAMOTIDINE 20 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (82804-194-78)
82804-194-90 82804-194 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20250204 N/A ANDA ANDA075718 Proficient Rx LP FAMOTIDINE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (82804-194-90)
55154-2628-0 55154-2628 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20230809 N/A ANDA ANDA075718 Cardinal Health 107, LLC FAMOTIDINE 20 mg/1 10 BLISTER PACK in 1 BAG (55154-2628-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
55154-4313-0 55154-4313 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20230315 N/A ANDA ANDA075718 Cardinal Health 107, LLC FAMOTIDINE 20 mg/1 10 BLISTER PACK in 1 BAG (55154-4313-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
50268-299-15 50268-299 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20220525 N/A ANDA ANDA075718 AvPAK FAMOTIDINE 20 mg/1 50 BLISTER PACK in 1 BOX (50268-299-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-299-11)
68788-8889-1 68788-8889 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20250923 N/A ANDA ANDA075718 Preferred Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-8889-1)
68788-8889-3 68788-8889 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20250923 N/A ANDA ANDA075718 Preferred Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8889-3)
68788-8889-6 68788-8889 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20250923 N/A ANDA ANDA075718 Preferred Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8889-6)
68788-8889-9 68788-8889 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20250923 N/A ANDA ANDA075718 Preferred Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8889-9)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase