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 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
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)
50090-4671-3 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 30 TABLET, FILM COATED in 1 BOTTLE (50090-4671-3)
50268-621-15 50268-621 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20160805 N/A ANDA ANDA078539 AvPAK ONDANSETRON HYDROCHLORIDE 4 mg/1 50 BLISTER PACK in 1 BOX (50268-621-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-621-11)
50268-622-15 50268-622 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20160805 N/A ANDA ANDA078539 AvPAK ONDANSETRON HYDROCHLORIDE 8 mg/1 50 BLISTER PACK in 1 BOX (50268-622-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-622-11)
51655-016-54 51655-016 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20220808 N/A ANDA ANDA078539 Northwind Pharmaceuticals, 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 Pharmaceuticals, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-87)
51655-016-27 51655-016 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20220916 N/A ANDA ANDA078539 Northwind Pharmaceuticals, 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 Pharmaceuticals, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-53)
51655-415-04 51655-415 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20180412 N/A ANDA ANDA078539 Northwind Pharmaceuticals, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 4 TABLET, FILM COATED in 1 BOTTLE (51655-415-04)
51655-415-55 51655-415 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20171207 N/A ANDA ANDA078539 Northwind Pharmaceuticals, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (51655-415-55)
51655-415-87 51655-415 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20181024 N/A ANDA ANDA078539 Northwind Pharmaceuticals, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (51655-415-87)
51655-813-54 51655-813 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20210610 N/A ANDA ANDA078539 Northwind Pharmaceuticals, LLC ONDANSETRON HYDROCHLORIDE 8 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-813-54)
51655-415-43 51655-415 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20171228 N/A ANDA ANDA078539 Northwind Pharmaceuticals, 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 Pharmaceuticals, 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 Pharmaceuticals, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (51655-415-54)
51655-933-04 51655-933 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20221025 N/A ANDA ANDA078539 Northwind Pharmaceuticals, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-04)
51655-933-55 51655-933 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20230509 N/A ANDA ANDA078539 Northwind Pharmaceuticals, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-55)
51655-933-87 51655-933 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20220720 N/A ANDA ANDA078539 Northwind Pharmaceuticals, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-87)
51655-933-43 51655-933 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20220720 N/A ANDA ANDA078539 Northwind Pharmaceuticals, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-43)
51655-933-53 51655-933 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20220916 N/A ANDA ANDA078539 Northwind Pharmaceuticals, LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-53)
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