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"
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
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)
72789-034-12 72789-034 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20191202 N/A ANDA ANDA078539 PD-Rx Pharmaceuticals, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-034-12)
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)
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)
80425-0074-6 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 9 TABLET, FILM COATED in 1 BOTTLE (80425-0074-6)
70518-3511-0 70518-3511 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20220906 N/A ANDA ANDA078539 REMEDYREPACK INC. ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3511-0)
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)
80425-0072-1 80425-0072 HUMAN PRESCRIPTION DRUG Ondansetron HCL Ondansetron HCL TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Advanced Rx of Tennessee, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (80425-0072-1)
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