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
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)
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)
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)
68788-8518-3 68788-8518 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20230901 N/A ANDA ANDA215630 Preferred Pharmaceuticals Inc. FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8518-3)
68788-8518-4 68788-8518 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20230901 N/A ANDA ANDA215630 Preferred Pharmaceuticals Inc. FAMOTIDINE 40 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (68788-8518-4)
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)
68788-8518-6 68788-8518 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20230901 N/A ANDA ANDA215630 Preferred Pharmaceuticals Inc. FAMOTIDINE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8518-6)
68788-8518-9 68788-8518 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20230901 N/A ANDA ANDA215630 Preferred Pharmaceuticals Inc. FAMOTIDINE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8518-9)
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)
76420-712-90 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)
76420-713-01 76420-713 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240411 N/A ANDA ANDA215630 Asclemed USA, Inc. FAMOTIDINE 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-713-01)
76420-713-30 76420-713 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET, FILM COATED ORAL 20240411 N/A ANDA ANDA215630 Asclemed USA, Inc. FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-713-30)
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