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=ANDA216441"
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
70710-1683-4 70710-1683 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20220606 N/A ANDA ANDA216441 Zydus Pharmaceuticals USA Inc. FAMOTIDINE 20 mg/1 10 BLISTER PACK in 1 CARTON (70710-1683-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1683-2)
70710-1683-5 70710-1683 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20220606 N/A ANDA ANDA216441 Zydus Pharmaceuticals USA Inc. FAMOTIDINE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (70710-1683-5)
70710-1684-0 70710-1684 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20220606 N/A ANDA ANDA216441 Zydus Pharmaceuticals USA Inc. FAMOTIDINE 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70710-1684-0)
70710-1684-1 70710-1684 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20220606 N/A ANDA ANDA216441 Zydus Pharmaceuticals USA Inc. FAMOTIDINE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1684-1)
70710-1684-3 70710-1684 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20220606 N/A ANDA ANDA216441 Zydus Pharmaceuticals USA Inc. FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70710-1684-3)
70710-1684-4 70710-1684 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20220606 N/A ANDA ANDA216441 Zydus Pharmaceuticals USA Inc. FAMOTIDINE 40 mg/1 10 BLISTER PACK in 1 CARTON (70710-1684-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1684-2)
70710-1684-5 70710-1684 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20220606 N/A ANDA ANDA216441 Zydus Pharmaceuticals USA Inc. FAMOTIDINE 40 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (70710-1684-5)
70710-1683-3 70710-1683 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20220606 N/A ANDA ANDA216441 Zydus Pharmaceuticals USA Inc. FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70710-1683-3)
70710-1683-1 70710-1683 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20220606 N/A ANDA ANDA216441 Zydus Pharmaceuticals USA Inc. FAMOTIDINE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1683-1)
70710-1683-0 70710-1683 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20220606 N/A ANDA ANDA216441 Zydus Pharmaceuticals USA Inc. FAMOTIDINE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70710-1683-0)
60760-736-07 60760-736 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20230206 N/A ANDA ANDA216441 ST. MARY'S MEDICAL PARK PHARMACY FAMOTIDINE 40 mg/1 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-736-07)
60760-736-60 60760-736 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20221208 N/A ANDA ANDA216441 ST. MARY'S MEDICAL PARK PHARMACY FAMOTIDINE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-736-60)
68071-3521-3 68071-3521 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20231012 N/A ANDA ANDA216441 NuCare Pharmaceuticals,Inc. FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3521-3)
71335-2190-2 71335-2190 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20221115 N/A ANDA ANDA216441 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-2190-2)
71335-2190-5 71335-2190 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20221115 N/A ANDA ANDA216441 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-2190-5)
71335-2190-6 71335-2190 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20221115 N/A ANDA ANDA216441 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71335-2190-6)
71335-2190-7 71335-2190 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20221115 N/A ANDA ANDA216441 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-2190-7)
71335-2190-8 71335-2190 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20221115 N/A ANDA ANDA216441 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (71335-2190-8)
71335-2190-9 71335-2190 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20221115 N/A ANDA ANDA216441 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71335-2190-9)
71335-2190-3 71335-2190 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20221115 N/A ANDA ANDA216441 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-2190-3)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase