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=ANDA078671"
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
51655-396-25 51655-396 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20200707 N/A ANDA ANDA078671 Northwind Pharmaceuticals, LLC NABUMETONE 500 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-396-25)
69097-966-07 69097-966 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20190306 N/A ANDA ANDA078671 Cipla USA Inc. NABUMETONE 750 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (69097-966-07)
69097-966-12 69097-966 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20190306 N/A ANDA ANDA078671 Cipla USA Inc. NABUMETONE 750 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (69097-966-12)
45865-464-60 45865-464 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20150826 N/A ANDA ANDA078671 Medsource Pharmaceuticals NABUMETONE 500 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (45865-464-60)
45865-464-90 45865-464 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20150826 N/A ANDA ANDA078671 Medsource Pharmaceuticals NABUMETONE 500 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (45865-464-90)
69097-965-07 69097-965 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20190306 N/A ANDA ANDA078671 Cipla USA Inc. NABUMETONE 500 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (69097-965-07)
69097-965-12 69097-965 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20190306 N/A ANDA ANDA078671 Cipla USA Inc. NABUMETONE 500 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (69097-965-12)
76282-258-01 76282-258 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20150414 N/A ANDA ANDA078671 Exelan Pharmaceuticals Inc. NABUMETONE 750 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76282-258-01)
76282-258-05 76282-258 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20150414 N/A ANDA ANDA078671 Exelan Pharmaceuticals Inc. NABUMETONE 750 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76282-258-05)
80425-0053-1 80425-0053 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20190306 N/A ANDA ANDA078671 Advanced Rx Pharmacy of Tennessee, LLC NABUMETONE 500 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0053-1)
50090-5386-0 50090-5386 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20201120 N/A ANDA ANDA078671 A-S Medication Solutions NABUMETONE 750 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-5386-0)
50090-5386-2 50090-5386 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20201120 N/A ANDA ANDA078671 A-S Medication Solutions NABUMETONE 750 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (50090-5386-2)
50090-5386-3 50090-5386 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20201120 N/A ANDA ANDA078671 A-S Medication Solutions NABUMETONE 750 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-5386-3)
50090-5386-4 50090-5386 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20201120 N/A ANDA ANDA078671 A-S Medication Solutions NABUMETONE 750 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (50090-5386-4)
76282-257-01 76282-257 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20150414 N/A ANDA ANDA078671 Exelan Pharmaceuticals Inc. NABUMETONE 500 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76282-257-01)
76282-257-05 76282-257 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20150414 N/A ANDA ANDA078671 Exelan Pharmaceuticals Inc. NABUMETONE 500 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76282-257-05)
63187-378-30 63187-378 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20160901 N/A ANDA ANDA078671 Proficient Rx LP NABUMETONE 750 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-378-30)
63187-378-60 63187-378 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20160901 N/A ANDA ANDA078671 Proficient Rx LP NABUMETONE 750 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-378-60)
60687-630-21 60687-630 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20220323 N/A ANDA ANDA078671 American Health Packaging NABUMETONE 500 mg/1 30 BLISTER PACK in 1 CARTON (60687-630-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-630-11)
63187-484-14 63187-484 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA078671 Proficient Rx LP NABUMETONE 500 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (63187-484-14)
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