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=ANDA078420"
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
60760-369-90 60760-369 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20210223 N/A ANDA ANDA078420 St. Mary's Medical Park Pharmacy NABUMETONE 750 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (60760-369-90)
60760-368-60 60760-368 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200303 N/A ANDA ANDA078420 St. Mary's Medical Park Pharmacy NABUMETONE 500 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (60760-368-60)
60760-369-14 60760-369 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20191010 N/A ANDA ANDA078420 St. Mary's Medical Park Pharmacy NABUMETONE 750 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (60760-369-14)
60760-369-60 60760-369 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200127 N/A ANDA ANDA078420 St. Mary's Medical Park Pharmacy NABUMETONE 750 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (60760-369-60)
68788-7597-3 68788-7597 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200213 N/A ANDA ANDA078420 Preferred Pharmaceuticals Inc. NABUMETONE 750 mg/1 30 TABLET in 1 BOTTLE (68788-7597-3)
68788-7597-6 68788-7597 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200213 N/A ANDA ANDA078420 Preferred Pharmaceuticals Inc. NABUMETONE 750 mg/1 60 TABLET in 1 BOTTLE (68788-7597-6)
68788-7597-8 68788-7597 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200213 N/A ANDA ANDA078420 Preferred Pharmaceuticals Inc. NABUMETONE 750 mg/1 120 TABLET in 1 BOTTLE (68788-7597-8)
68788-7597-9 68788-7597 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200213 N/A ANDA ANDA078420 Preferred Pharmaceuticals Inc. NABUMETONE 750 mg/1 90 TABLET in 1 BOTTLE (68788-7597-9)
68788-7597-1 68788-7597 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200213 N/A ANDA ANDA078420 Preferred Pharmaceuticals Inc. NABUMETONE 750 mg/1 100 TABLET in 1 BOTTLE (68788-7597-1)
68788-7597-2 68788-7597 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200213 N/A ANDA ANDA078420 Preferred Pharmaceuticals Inc. NABUMETONE 750 mg/1 20 TABLET in 1 BOTTLE (68788-7597-2)
68788-7765-3 68788-7765 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200715 N/A ANDA ANDA078420 Preferred Pharmaceuticals, Inc. NABUMETONE 500 mg/1 30 TABLET in 1 BOTTLE (68788-7765-3)
68788-7765-8 68788-7765 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200715 N/A ANDA ANDA078420 Preferred Pharmaceuticals, Inc. NABUMETONE 500 mg/1 120 TABLET in 1 BOTTLE (68788-7765-8)
68788-7765-9 68788-7765 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200715 N/A ANDA ANDA078420 Preferred Pharmaceuticals, Inc. NABUMETONE 500 mg/1 90 TABLET in 1 BOTTLE (68788-7765-9)
68788-7765-6 68788-7765 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200715 N/A ANDA ANDA078420 Preferred Pharmaceuticals, Inc. NABUMETONE 500 mg/1 60 TABLET in 1 BOTTLE (68788-7765-6)
68788-7765-1 68788-7765 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200715 N/A ANDA ANDA078420 Preferred Pharmaceuticals, Inc. NABUMETONE 500 mg/1 100 TABLET in 1 BOTTLE (68788-7765-1)
68788-7765-2 68788-7765 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200715 N/A ANDA ANDA078420 Preferred Pharmaceuticals, Inc. NABUMETONE 500 mg/1 20 TABLET in 1 BOTTLE (68788-7765-2)
71205-530-30 71205-530 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20210203 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 750 mg/1 30 TABLET in 1 BOTTLE (71205-530-30)
71205-530-60 71205-530 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20210203 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 750 mg/1 60 TABLET in 1 BOTTLE (71205-530-60)
71205-530-90 71205-530 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20210203 N/A ANDA ANDA078420 Proficient Rx LP NABUMETONE 750 mg/1 90 TABLET in 1 BOTTLE (71205-530-90)
55700-845-60 55700-845 HUMAN PRESCRIPTION DRUG Nabumetone Nabumetone TABLET ORAL 20200228 20270331 ANDA ANDA078420 Quality Care Products, LLC NABUMETONE 500 mg/1 60 TABLET in 1 BOTTLE (55700-845-60)
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