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=ANDA204770"
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
85509-1435-9 85509-1435 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20251016 N/A ANDA ANDA204770 PHOENIX RX LLC METAXALONE 800 mg/1 90 TABLET in 1 BOTTLE (85509-1435-9)
61919-832-90 61919-832 HUMAN PRESCRIPTION DRUG METAXALONE METAXALONE TABLET ORAL 20190503 N/A ANDA ANDA204770 DIRECT RX METAXALONE 800 mg/1 90 TABLET in 1 BOTTLE (61919-832-90)
68788-7675-0 68788-7675 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20200302 N/A ANDA ANDA204770 Preferred Pharmaceuticals, Inc. METAXALONE 800 mg/1 15 TABLET in 1 BOTTLE (68788-7675-0)
68788-7675-1 68788-7675 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20200302 N/A ANDA ANDA204770 Preferred Pharmaceuticals, Inc. METAXALONE 800 mg/1 100 TABLET in 1 BOTTLE (68788-7675-1)
68788-7675-2 68788-7675 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20200302 N/A ANDA ANDA204770 Preferred Pharmaceuticals, Inc. METAXALONE 800 mg/1 20 TABLET in 1 BOTTLE (68788-7675-2)
68788-7675-3 68788-7675 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20200302 N/A ANDA ANDA204770 Preferred Pharmaceuticals, Inc. METAXALONE 800 mg/1 30 TABLET in 1 BOTTLE (68788-7675-3)
68788-7675-6 68788-7675 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20200302 N/A ANDA ANDA204770 Preferred Pharmaceuticals, Inc. METAXALONE 800 mg/1 60 TABLET in 1 BOTTLE (68788-7675-6)
68788-7675-9 68788-7675 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20200302 N/A ANDA ANDA204770 Preferred Pharmaceuticals, Inc. METAXALONE 800 mg/1 90 TABLET in 1 BOTTLE (68788-7675-9)
0527-1435-01 0527-1435 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20161122 N/A ANDA ANDA204770 Lannett Company, Inc. METAXALONE 800 mg/1 100 TABLET in 1 BOTTLE (0527-1435-01)
0527-1435-05 0527-1435 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20161122 N/A ANDA ANDA204770 Lannett Company, Inc. METAXALONE 800 mg/1 500 TABLET in 1 BOTTLE (0527-1435-05)
69306-311-20 69306-311 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20220325 N/A ANDA ANDA204770 Doc Rx METAXALONE 800 mg/1 20 TABLET in 1 BOTTLE (69306-311-20)
69306-311-30 69306-311 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20220325 N/A ANDA ANDA204770 Doc Rx METAXALONE 800 mg/1 30 TABLET in 1 BOTTLE (69306-311-30)
69306-311-60 69306-311 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20220325 N/A ANDA ANDA204770 Doc Rx METAXALONE 800 mg/1 60 TABLET in 1 BOTTLE (69306-311-60)
69306-311-90 69306-311 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20220325 N/A ANDA ANDA204770 Doc Rx METAXALONE 800 mg/1 90 TABLET in 1 BOTTLE (69306-311-90)
50090-3650-0 50090-3650 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20181011 N/A ANDA ANDA204770 A-S Medication Solutions METAXALONE 800 mg/1 30 TABLET in 1 BOTTLE (50090-3650-0)
50090-3650-1 50090-3650 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20181011 N/A ANDA ANDA204770 A-S Medication Solutions METAXALONE 800 mg/1 60 TABLET in 1 BOTTLE (50090-3650-1)
50090-3650-2 50090-3650 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20161122 N/A ANDA ANDA204770 A-S Medication Solutions METAXALONE 800 mg/1 15 TABLET in 1 BOTTLE, PLASTIC (50090-3650-2)
50090-3650-3 50090-3650 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20161122 N/A ANDA ANDA204770 A-S Medication Solutions METAXALONE 800 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (50090-3650-3)
50090-3650-4 50090-3650 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20161122 N/A ANDA ANDA204770 A-S Medication Solutions METAXALONE 800 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (50090-3650-4)
50090-3650-5 50090-3650 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20181018 N/A ANDA ANDA204770 A-S Medication Solutions METAXALONE 800 mg/1 100 TABLET in 1 BOTTLE (50090-3650-5)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase