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=ANDA078539"
符合检索条件的记录共 255 条，共 13 页，当前第 3 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
50090-4671-1 50090-4671 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20191101 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (50090-4671-1)
50090-4671-2 50090-4671 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20191101 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (50090-4671-2)
50090-4671-3 50090-4671 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20191101 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-4671-3)
50090-4671-4 50090-4671 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20191101 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (50090-4671-4)
71335-0205-6 71335-0205 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20211227 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 4 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (71335-0205-6)
50090-3185-3 50090-3185 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-3)
50090-3185-4 50090-3185 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-4)
85766-053-05 85766-053 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20251001 N/A ANDA ANDA078539 Sportpharm, Inc. dba Sportpharm ONDANSETRON HYDROCHLORIDE 8 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (85766-053-05)
85766-053-10 85766-053 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20251001 N/A ANDA ANDA078539 Sportpharm, Inc. dba Sportpharm ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (85766-053-10)
85766-053-14 85766-053 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20251001 N/A ANDA ANDA078539 Sportpharm, Inc. dba Sportpharm ONDANSETRON HYDROCHLORIDE 8 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (85766-053-14)
85766-053-20 85766-053 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20251001 N/A ANDA ANDA078539 Sportpharm, Inc. dba Sportpharm ONDANSETRON HYDROCHLORIDE 8 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (85766-053-20)
85766-053-24 85766-053 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20251001 N/A ANDA ANDA078539 Sportpharm, Inc. dba Sportpharm ONDANSETRON HYDROCHLORIDE 8 mg/1 24 TABLET, FILM COATED in 1 BOTTLE (85766-053-24)
85766-053-30 85766-053 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20251001 N/A ANDA ANDA078539 Sportpharm, Inc. dba Sportpharm ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (85766-053-30)
85766-053-60 85766-053 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20251001 N/A ANDA ANDA078539 Sportpharm, Inc. dba Sportpharm ONDANSETRON HYDROCHLORIDE 8 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (85766-053-60)
71335-0205-7 71335-0205 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180216 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 4 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0205-7)
71335-0205-8 71335-0205 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180301 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 4 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (71335-0205-8)
71335-0205-9 71335-0205 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180403 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 4 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-0205-9)
70518-4145-0 70518-4145 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240718 N/A ANDA ANDA078539 REMEDYREPACK INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 16 TABLET, FILM COATED in 1 BLISTER PACK (70518-4145-0)
70518-4145-1 70518-4145 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240718 N/A ANDA ANDA078539 REMEDYREPACK INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4145-1)
70518-4145-2 70518-4145 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20241220 N/A ANDA ANDA078539 REMEDYREPACK INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4145-2)
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