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=ANDA075805"
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
53002-3199-0 53002-3199 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20210101 N/A ANDA ANDA075805 RPK Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 100 TABLET in 1 BOTTLE (53002-3199-0)
72789-027-60 72789-027 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20191211 N/A ANDA ANDA075805 PD-Rx Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (72789-027-60)
72789-027-30 72789-027 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20191211 N/A ANDA ANDA075805 PD-Rx Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (72789-027-30)
53002-6672-3 53002-6672 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20240101 N/A ANDA ANDA075805 RPK Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 30 TABLET in 1 BOTTLE (53002-6672-3)
63739-645-10 63739-645 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20150129 N/A ANDA ANDA075805 Mckesson Corporation DBA SKY Packaginng FAMOTIDINE 20 mg/1 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-645-10) / 10 TABLET in 1 BLISTER PACK
53002-6672-1 53002-6672 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20240101 N/A ANDA ANDA075805 RPK Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 10 TABLET in 1 BOTTLE (53002-6672-1)
53002-6672-6 53002-6672 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20240101 N/A ANDA ANDA075805 RPK Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 60 TABLET in 1 BOTTLE (53002-6672-6)
53002-6672-2 53002-6672 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20240101 N/A ANDA ANDA075805 RPK Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 20 TABLET in 1 BOTTLE (53002-6672-2)
61919-281-20 61919-281 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET ORAL 20190808 N/A ANDA ANDA075805 Direct_Rx FAMOTIDINE 20 mg/1 20 TABLET in 1 BOTTLE (61919-281-20)
61919-281-30 61919-281 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET ORAL 20190808 N/A ANDA ANDA075805 Direct_Rx FAMOTIDINE 20 mg/1 30 TABLET in 1 BOTTLE (61919-281-30)
61919-281-90 61919-281 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET ORAL 20190808 N/A ANDA ANDA075805 Direct_Rx FAMOTIDINE 20 mg/1 90 TABLET in 1 BOTTLE (61919-281-90)
63629-1013-1 63629-1013 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20120410 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 100 TABLET in 1 BOTTLE (63629-1013-1)
63629-1013-5 63629-1013 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20120410 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 500 TABLET in 1 BOTTLE (63629-1013-5)
63629-1013-6 63629-1013 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20120410 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 60 TABLET in 1 BOTTLE (63629-1013-6)
63629-1013-8 63629-1013 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20120410 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 800 TABLET in 1 BOTTLE (63629-1013-8)
63629-1014-0 63629-1014 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20110525 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 1000 TABLET in 1 BOTTLE (63629-1014-0)
63629-1014-1 63629-1014 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20110525 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 100 TABLET in 1 BOTTLE (63629-1014-1)
63629-1014-2 63629-1014 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20110525 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 30 TABLET in 1 BOTTLE (63629-1014-2)
63629-1014-3 63629-1014 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20110525 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 300 TABLET in 1 BOTTLE (63629-1014-3)
63629-1014-5 63629-1014 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20110525 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 500 TABLET in 1 BOTTLE (63629-1014-5)
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