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"
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
68788-8485-3 68788-8485 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20230718 N/A ANDA ANDA215630 Preferred Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8485-3)
68788-8485-4 68788-8485 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20230718 N/A ANDA ANDA215630 Preferred Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (68788-8485-4)
68788-8485-6 68788-8485 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20230718 N/A ANDA ANDA215630 Preferred Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8485-6)
68788-8485-9 68788-8485 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20230718 N/A ANDA ANDA215630 Preferred Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8485-9)
76420-712-01 76420-712 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240411 N/A ANDA ANDA215630 Asclemed USA, Inc. FAMOTIDINE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-712-01)
76420-712-30 76420-712 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240411 N/A ANDA ANDA215630 Asclemed USA, Inc. FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-712-30)
76420-712-60 76420-712 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240411 N/A ANDA ANDA215630 Asclemed USA, Inc. FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-712-60)
76420-712-90 76420-712 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240411 N/A ANDA ANDA215630 Asclemed USA, Inc. FAMOTIDINE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-712-90)
71335-9748-1 71335-9748 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20230914 N/A ANDA ANDA215630 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-9748-1)
71335-9748-2 71335-9748 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20231003 N/A ANDA ANDA215630 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-9748-2)
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)
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)
68071-3584-3 68071-3584 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240307 N/A ANDA ANDA215630 NuCare Pharmaceuticals,Inc. FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3584-3)
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)
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)
70518-3829-4 70518-3829 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240228 N/A ANDA ANDA215630 REMEDYREPACK INC. FAMOTIDINE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-4)
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