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 262 条，共 14 页，当前第 13 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
68071-4328-4 68071-4328 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180312 N/A ANDA ANDA078539 NuCare Pharmceuticals,Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (68071-4328-4)
76420-917-01 76420-917 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 24 mg/1 1 BLISTER PACK in 1 CARTON (76420-917-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK
80425-0074-1 80425-0074 HUMAN PRESCRIPTION DRUG Ondansetron HCL Ondansetron HCL TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA078539 Advanced Rx of Tennessee, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (80425-0074-1)
80425-0074-2 80425-0074 HUMAN PRESCRIPTION DRUG Ondansetron HCL Ondansetron HCL TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA078539 Advanced Rx of Tennessee, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (80425-0074-2)
80425-0074-3 80425-0074 HUMAN PRESCRIPTION DRUG Ondansetron HCL Ondansetron HCL TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA078539 Advanced Rx of Tennessee, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (80425-0074-3)
80425-0074-4 80425-0074 HUMAN PRESCRIPTION DRUG Ondansetron HCL Ondansetron HCL TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA078539 Advanced Rx of Tennessee, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0074-4)
80425-0074-5 80425-0074 HUMAN PRESCRIPTION DRUG Ondansetron HCL Ondansetron HCL TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA078539 Advanced Rx of Tennessee, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0074-5)
71335-0205-0 71335-0205 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180405 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 4 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0205-0)
71335-0205-1 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 10 TABLET, FILM COATED in 1 BOTTLE (71335-0205-1)
71335-0205-2 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 3 TABLET, FILM COATED in 1 BOTTLE (71335-0205-2)
71335-0205-3 71335-0205 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180308 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0205-3)
71335-0205-4 71335-0205 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180214 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 4 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-0205-4)
71335-0205-5 71335-0205 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180321 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 4 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (71335-0205-5)
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)
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)
68084-220-01 68084-220 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20230921 N/A ANDA ANDA078539 American Health Packaging ONDANSETRON HYDROCHLORIDE 4 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-220-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-220-11)
65862-188-05 65862-188 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Aurobindo Pharma Limited ONDANSETRON HYDROCHLORIDE 8 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-188-05)
65862-188-10 65862-188 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Aurobindo Pharma Limited ONDANSETRON HYDROCHLORIDE 8 mg/1 10 BLISTER PACK in 1 CARTON (65862-188-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase