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 10 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
85509-1075-3 85509-1075 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250731 N/A ANDA ANDA078539 PHOENIX RX LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (85509-1075-3)
85509-1075-4 85509-1075 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250731 N/A ANDA ANDA078539 PHOENIX RX LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (85509-1075-4)
85509-1075-5 85509-1075 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250731 N/A ANDA ANDA078539 PHOENIX RX LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (85509-1075-5)
85509-1075-6 85509-1075 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250731 N/A ANDA ANDA078539 PHOENIX RX LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (85509-1075-6)
85509-1076-1 85509-1076 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250731 N/A ANDA ANDA078539 PHOENIX RX LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (85509-1076-1)
85509-1076-2 85509-1076 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250731 N/A ANDA ANDA078539 PHOENIX RX LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (85509-1076-2)
85509-1076-3 85509-1076 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250731 N/A ANDA ANDA078539 PHOENIX RX LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (85509-1076-3)
85509-1076-5 85509-1076 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250731 N/A ANDA ANDA078539 PHOENIX RX LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (85509-1076-5)
85509-1076-6 85509-1076 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250731 N/A ANDA ANDA078539 PHOENIX RX LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (85509-1076-6)
72162-2364-5 72162-2364 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240716 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 4 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72162-2364-5)
72162-2365-5 72162-2365 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240716 N/A ANDA ANDA078539 Bryant Ranch Prepack ONDANSETRON HYDROCHLORIDE 8 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72162-2365-5)
85509-1057-4 85509-1057 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250731 N/A ANDA ANDA078539 PHOENIX RX LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (85509-1057-4)
70518-1585-3 70518-1585 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20230801 N/A ANDA ANDA078539 REMEDYREPACK INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1585-3)
83008-074-30 83008-074 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240725 20280131 ANDA ANDA078539 Quality Care Products, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (83008-074-30)
70518-1585-6 70518-1585 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20251001 N/A ANDA ANDA078539 REMEDYREPACK INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1585-6)
83008-074-20 83008-074 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20240725 20280131 ANDA ANDA078539 Quality Care Products, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (83008-074-20)
70518-1585-2 70518-1585 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20210203 N/A ANDA ANDA078539 REMEDYREPACK INC. ONDANSETRON HYDROCHLORIDE 4 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1585-2)
85766-006-00 85766-006 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250619 N/A ANDA ANDA078539 Sportpharm, Inc. dba Sportpharm ONDANSETRON HYDROCHLORIDE 4 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (85766-006-00)
85766-006-10 85766-006 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20250619 N/A ANDA ANDA078539 Sportpharm, Inc. dba Sportpharm ONDANSETRON HYDROCHLORIDE 4 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (85766-006-10)
85766-006-24 85766-006 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20251001 N/A ANDA ANDA078539 Sportpharm, Inc. dba Sportpharm ONDANSETRON HYDROCHLORIDE 4 mg/1 24 TABLET, FILM COATED in 1 BOTTLE (85766-006-24)
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