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 247 条，共 13 页，当前第 6 页 ，可点击列名称排序
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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
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)
80425-0075-1 80425-0075 HUMAN PRESCRIPTION DRUG Ondansetron HCL Ondansetron HCL TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Advanced Rx of Tennessee, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (80425-0075-1)
80425-0075-2 80425-0075 HUMAN PRESCRIPTION DRUG Ondansetron HCL Ondansetron HCL TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Advanced Rx of Tennessee, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (80425-0075-2)
80425-0075-3 80425-0075 HUMAN PRESCRIPTION DRUG Ondansetron HCL Ondansetron HCL TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Advanced Rx of Tennessee, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (80425-0075-3)
80425-0075-4 80425-0075 HUMAN PRESCRIPTION DRUG Ondansetron HCL Ondansetron HCL TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Advanced Rx of Tennessee, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0075-4)
80425-0075-5 80425-0075 HUMAN PRESCRIPTION DRUG Ondansetron HCL Ondansetron HCL TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Advanced Rx of Tennessee, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0075-5)
16714-159-01 16714-159 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET, FILM COATED ORAL 20210406 N/A ANDA ANDA078539 NorthStar Rx LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16714-159-01)
16714-160-01 16714-160 HUMAN PRESCRIPTION DRUG Ondansetron Ondansetron TABLET, FILM COATED ORAL 20210406 N/A ANDA ANDA078539 NorthStar Rx LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16714-160-01)
42708-044-05 42708-044 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180405 N/A ANDA ANDA078539 QPharma, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (42708-044-05)
42708-059-05 42708-059 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180419 N/A ANDA ANDA078539 QPharma, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (42708-059-05)
42708-179-05 42708-179 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20230519 N/A ANDA ANDA078539 QPharma, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-179-05)
43063-792-06 43063-792 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20171006 N/A ANDA ANDA078539 PD-Rx Pharmaceuticals, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-792-06)
50090-3178-0 50090-3178 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20171106 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 4 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (50090-3178-0)
50090-3178-1 50090-3178 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 4 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3178-1)
50090-3178-2 50090-3178 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 4 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3178-2)
50090-3178-4 50090-3178 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 4 mg/1 3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3178-4)
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