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
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)
71335-2442-1 71335-2442 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240715 N/A ANDA ANDA215630 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2442-1)
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)
71335-2442-2 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)
71335-2442-6 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)
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)
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