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 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
80425-0075-2 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)
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
68788-9402-6 68788-9402 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20170623 N/A ANDA ANDA078539 Preferred Pharmaceuticals, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (68788-9402-6)
51655-016-27 51655-016 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20220916 N/A ANDA ANDA078539 Northwind Health Company, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-27)
51655-016-53 51655-016 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20220916 N/A ANDA ANDA078539 Northwind Health Company, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-53)
51655-016-54 51655-016 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20220808 N/A ANDA ANDA078539 Northwind Health Company, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-54)
51655-016-87 51655-016 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20220921 N/A ANDA ANDA078539 Northwind Health Company, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-87)
76420-411-00 76420-411 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250619 N/A ANDA ANDA078539 ASCLEMED USA INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76420-411-00)
76420-411-03 76420-411 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250619 N/A ANDA ANDA078539 ASCLEMED USA INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (76420-411-03)
76420-411-05 76420-411 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250619 N/A ANDA ANDA078539 ASCLEMED USA INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-411-05)
76420-411-06 76420-411 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250619 N/A ANDA ANDA078539 ASCLEMED USA INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (76420-411-06)
76420-411-08 76420-411 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20260405 N/A ANDA ANDA078539 ASCLEMED USA INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 8 TABLET, FILM COATED in 1 BOTTLE (76420-411-08)
76420-411-10 76420-411 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250619 N/A ANDA ANDA078539 ASCLEMED USA INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (76420-411-10)
76420-411-24 76420-411 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20251001 N/A ANDA ANDA078539 ASCLEMED USA INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 24 TABLET, FILM COATED in 1 BOTTLE (76420-411-24)
76420-411-30 76420-411 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250619 N/A ANDA ANDA078539 ASCLEMED USA INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-411-30)
76420-411-60 76420-411 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250619 N/A ANDA ANDA078539 ASCLEMED USA INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-411-60)
76420-411-90 76420-411 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250619 N/A ANDA ANDA078539 ASCLEMED USA INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-411-90)
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