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 12 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
76420-915-05 76420-915 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-915-05)
76420-915-10 76420-915 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (76420-915-10)
76420-915-11 76420-915 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 10 BLISTER PACK in 1 CARTON (76420-915-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK
76420-915-30 76420-915 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-915-30)
76420-915-33 76420-915 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 1 BLISTER PACK in 1 CARTON (76420-915-33) / 3 TABLET, FILM COATED in 1 BLISTER PACK
76420-915-60 76420-915 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-915-60)
76420-915-90 76420-915 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA078539 Asclemed USA, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-915-90)
68788-8582-1 68788-8582 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240212 N/A ANDA ANDA078539 Preferred Pharmaceuticals Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (68788-8582-1)
68788-8582-2 68788-8582 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240212 N/A ANDA ANDA078539 Preferred Pharmaceuticals Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (68788-8582-2)
68788-8582-3 68788-8582 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240212 N/A ANDA ANDA078539 Preferred Pharmaceuticals Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8582-3)
68788-8582-5 68788-8582 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240212 N/A ANDA ANDA078539 Preferred Pharmaceuticals Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68788-8582-5)
68788-8582-6 68788-8582 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240212 N/A ANDA ANDA078539 Preferred Pharmaceuticals Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8582-6)
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)
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
65862-188-30 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 30 TABLET, FILM COATED in 1 BOTTLE (65862-188-30)
65862-188-99 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 1000 TABLET, FILM COATED in 1 BOTTLE (65862-188-99)
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)
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