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 7 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
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)
57237-075-30 57237-075 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Rising Pharma Holdings, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (57237-075-30)
57237-075-50 57237-075 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20221004 N/A ANDA ANDA078539 Rising Pharma Holdings, Inc. ONDANSETRON HYDROCHLORIDE 4 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (57237-075-50)
57237-076-30 57237-076 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Rising Pharma Holdings, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (57237-076-30)
57237-076-50 57237-076 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20221004 N/A ANDA ANDA078539 Rising Pharma Holdings, Inc. ONDANSETRON HYDROCHLORIDE 8 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (57237-076-50)
61919-565-30 61919-565 HUMAN PRESCRIPTION DRUG ONDANSETRON ONDANSETRON TABLET, FILM COATED ORAL 20190822 N/A ANDA ANDA078539 Direct_Rx ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (61919-565-30)
65862-187-03 65862-187 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Aurobindo Pharma Limited ONDANSETRON HYDROCHLORIDE 4 mg/1 1 BLISTER PACK in 1 CARTON (65862-187-03) / 3 TABLET, FILM COATED in 1 BLISTER PACK
65862-187-05 65862-187 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Aurobindo Pharma Limited ONDANSETRON HYDROCHLORIDE 4 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-187-05)
65862-187-10 65862-187 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Aurobindo Pharma Limited ONDANSETRON HYDROCHLORIDE 4 mg/1 10 BLISTER PACK in 1 CARTON (65862-187-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
65862-187-30 65862-187 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Aurobindo Pharma Limited ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-187-30)
65862-187-99 65862-187 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Aurobindo Pharma Limited ONDANSETRON HYDROCHLORIDE 4 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-187-99)
65862-188-03 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 1 BLISTER PACK in 1 CARTON (65862-188-03) / 3 TABLET, FILM COATED in 1 BLISTER PACK
65862-188-05 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/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-188-05)
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)
65862-189-11 65862-189 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20070731 N/A ANDA ANDA078539 Aurobindo Pharma Limited ONDANSETRON HYDROCHLORIDE 24 mg/1 1 BLISTER PACK in 1 CARTON (65862-189-11) / 1 TABLET, FILM COATED in 1 BLISTER PACK
67046-0346-3 67046-0346 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20241108 N/A ANDA ANDA078539 Coupler LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-0346-3)
67046-0346-6 67046-0346 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20241108 N/A ANDA ANDA078539 Coupler LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 60 TABLET, FILM COATED in 1 BLISTER PACK (67046-0346-6)
67046-1029-3 67046-1029 HUMAN PRESCRIPTION DRUG Ondansetron Hydrochloride Ondansetron Hydrochloride TABLET, FILM COATED ORAL 20241111 N/A ANDA ANDA078539 Coupler LLC ONDANSETRON HYDROCHLORIDE 4 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1029-3)
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