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=ANDA075511"
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
71205-276-60 71205-276 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20190501 N/A ANDA ANDA075511 Proficient Rx LP FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-276-60)
71205-276-67 71205-276 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20240923 N/A ANDA ANDA075511 Proficient Rx LP FAMOTIDINE 20 mg/1 270 TABLET, FILM COATED in 1 BOTTLE (71205-276-67)
71205-276-78 71205-276 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20250710 N/A ANDA ANDA075511 Proficient Rx LP FAMOTIDINE 20 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71205-276-78)
50090-6932-0 50090-6932 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20231214 N/A ANDA ANDA075511 A-S Medication Solutions FAMOTIDINE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6932-0)
68645-140-59 68645-140 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20091026 N/A ANDA ANDA075511 Legacy Pharmaceutical Packaging, LLC FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68645-140-59)
71205-781-30 71205-781 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20230327 N/A ANDA ANDA075511 Proficient Rx LP FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-781-30)
71205-781-60 71205-781 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20230327 N/A ANDA ANDA075511 Proficient Rx LP FAMOTIDINE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-781-60)
71205-781-90 71205-781 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20230327 N/A ANDA ANDA075511 Proficient Rx LP FAMOTIDINE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-781-90)
0172-5728-60 0172-5728 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20010416 N/A ANDA ANDA075511 Teva Pharmaceuticals USA, Inc. FAMOTIDINE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0172-5728-60)
0172-5728-70 0172-5728 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20010416 N/A ANDA ANDA075511 Teva Pharmaceuticals USA, Inc. FAMOTIDINE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (0172-5728-70)
0172-5728-80 0172-5728 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20010416 N/A ANDA ANDA075511 Teva Pharmaceuticals USA, Inc. FAMOTIDINE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (0172-5728-80)
0172-5729-60 0172-5729 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20010416 N/A ANDA ANDA075511 Teva Pharmaceuticals USA, Inc. FAMOTIDINE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0172-5729-60)
0172-5729-70 0172-5729 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20010416 N/A ANDA ANDA075511 Teva Pharmaceuticals USA, Inc. FAMOTIDINE 40 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (0172-5729-70)
50090-1044-0 50090-1044 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA075511 A-S Medication Solutions FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-1044-0)
50090-1044-1 50090-1044 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA075511 A-S Medication Solutions FAMOTIDINE 20 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (50090-1044-1)
50090-1044-2 50090-1044 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA075511 A-S Medication Solutions FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-1044-2)
50090-1044-3 50090-1044 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20181005 N/A ANDA ANDA075511 A-S Medication Solutions FAMOTIDINE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-1044-3)
51655-102-26 51655-102 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20230125 N/A ANDA ANDA075511 Northwind Health Company, LLC FAMOTIDINE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-102-26)
51655-102-30 51655-102 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20140825 N/A ANDA ANDA075511 Northwind Health Company, LLC FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-102-30)
51655-233-25 51655-233 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20221206 N/A ANDA ANDA075511 Northwind Health Company, LLC FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-233-25)
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