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=ANDA215630"
符合检索条件的记录共 73 条，共 4 页，当前第 2 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
50090-7829-0 50090-7829 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20251217 N/A ANDA ANDA215630 A-S Medication Solutions FAMOTIDINE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-7829-0)
70518-4084-1 70518-4084 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20250529 N/A ANDA ANDA215630 REMEDYREPACK INC. FAMOTIDINE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4084-1)
70518-4084-2 70518-4084 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20251012 N/A ANDA ANDA215630 REMEDYREPACK INC. FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4084-2)
72789-345-30 72789-345 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20230807 N/A ANDA ANDA215630 PD-Rx Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-345-30)
70518-3829-1 70518-3829 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20231106 N/A ANDA ANDA215630 REMEDYREPACK INC. FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-1)
71335-2442-2 71335-2442 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240715 N/A ANDA ANDA215630 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-2442-2)
71335-2442-3 71335-2442 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240715 N/A ANDA ANDA215630 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-2442-3)
71335-2442-4 71335-2442 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240715 N/A ANDA ANDA215630 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-2442-4)
71335-2442-5 71335-2442 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240715 N/A ANDA ANDA215630 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-2442-5)
71335-2442-6 71335-2442 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240715 N/A ANDA ANDA215630 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-2442-6)
71335-2442-7 71335-2442 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240715 N/A ANDA ANDA215630 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-2442-7)
71335-2442-8 71335-2442 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240715 N/A ANDA ANDA215630 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71335-2442-8)
72789-453-30 72789-453 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20241114 N/A ANDA ANDA215630 PD-Rx Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-453-30)
68071-3413-3 68071-3413 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20230523 N/A ANDA ANDA215630 NuCare Pharmceuticals,Inc. FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3413-3)
68071-3420-3 68071-3420 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20230726 N/A ANDA ANDA215630 NuCare Pharmaceuticals,Inc. FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3420-3)
68071-3420-6 68071-3420 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20230601 N/A ANDA ANDA215630 NuCare Pharmaceuticals,Inc. FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-3420-6)
68071-3420-7 68071-3420 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20230726 N/A ANDA ANDA215630 NuCare Pharmaceuticals,Inc. FAMOTIDINE 20 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (68071-3420-7)
68071-3420-8 68071-3420 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20230726 N/A ANDA ANDA215630 NuCare Pharmaceuticals,Inc. FAMOTIDINE 20 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (68071-3420-8)
68071-3420-9 68071-3420 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20230726 N/A ANDA ANDA215630 NuCare Pharmaceuticals,Inc. FAMOTIDINE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-3420-9)
70518-3829-3 70518-3829 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240124 N/A ANDA ANDA215630 REMEDYREPACK INC. FAMOTIDINE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-3)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase