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 5 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
50090-4671-1 50090-4671 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20191101 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (50090-4671-1)
50090-3185-1 50090-3185 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-1)
50090-3185-2 50090-3185 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-2)
50090-3185-3 50090-3185 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-3)
50090-3185-4 50090-3185 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3185-4)
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)
68071-1742-3 68071-1742 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20230406 N/A ANDA ANDA078539 NuCare Pharmaceuticals,Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-1742-3)
55700-627-10 55700-627 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180518 20270630 ANDA ANDA078539 Quality Care Products LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (55700-627-10)
55700-627-20 55700-627 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180518 20270630 ANDA ANDA078539 Quality Care Products LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (55700-627-20)
55700-627-30 55700-627 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180518 20280131 ANDA ANDA078539 Quality Care Products LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (55700-627-30)
68071-5047-3 68071-5047 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20190904 N/A ANDA ANDA078539 NuCare Pharmaceuticals,Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-5047-3)
51655-415-04 51655-415 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180412 N/A ANDA ANDA078539 Northwind Health Company, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (51655-415-04)
51655-415-43 51655-415 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20171228 N/A ANDA ANDA078539 Northwind Health Company, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (51655-415-43)
51655-415-53 51655-415 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180424 N/A ANDA ANDA078539 Northwind Health Company, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (51655-415-53)
51655-415-54 51655-415 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20171228 N/A ANDA ANDA078539 Northwind Health Company, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (51655-415-54)
51655-415-55 51655-415 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20171207 N/A ANDA ANDA078539 Northwind Health Company, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (51655-415-55)
50090-4671-2 50090-4671 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20191101 N/A ANDA ANDA078539 A-S Medication Solutions ONDANSETRON HYDROCHLORIDE 8 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (50090-4671-2)
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