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=ANDA203695"
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
72189-645-30 72189-645 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20251208 N/A ANDA ANDA203695 Direct_Rx METAXALONE 800 mg/1 30 TABLET in 1 BOTTLE (72189-645-30)
72189-645-60 72189-645 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20251208 N/A ANDA ANDA203695 Direct_Rx METAXALONE 800 mg/1 60 TABLET in 1 BOTTLE (72189-645-60)
72189-645-90 72189-645 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20251208 N/A ANDA ANDA203695 Direct_Rx METAXALONE 800 mg/1 90 TABLET in 1 BOTTLE (72189-645-90)
71205-326-20 71205-326 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20200930 N/A ANDA ANDA203695 Proficient Rx LP METAXALONE 800 mg/1 20 TABLET in 1 BOTTLE (71205-326-20)
71205-326-30 71205-326 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20190901 N/A ANDA ANDA203695 Proficient Rx LP METAXALONE 800 mg/1 30 TABLET in 1 BOTTLE (71205-326-30)
71205-326-60 71205-326 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20190901 N/A ANDA ANDA203695 Proficient Rx LP METAXALONE 800 mg/1 60 TABLET in 1 BOTTLE (71205-326-60)
71205-326-90 71205-326 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20190901 N/A ANDA ANDA203695 Proficient Rx LP METAXALONE 800 mg/1 90 TABLET in 1 BOTTLE (71205-326-90)
76420-898-20 76420-898 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20250110 N/A ANDA ANDA203695 Asclemed USA, Inc. METAXALONE 800 mg/1 20 TABLET in 1 BOTTLE (76420-898-20)
76420-898-30 76420-898 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20250110 N/A ANDA ANDA203695 Asclemed USA, Inc. METAXALONE 800 mg/1 30 TABLET in 1 BOTTLE (76420-898-30)
76420-898-60 76420-898 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20250110 N/A ANDA ANDA203695 Asclemed USA, Inc. METAXALONE 800 mg/1 60 TABLET in 1 BOTTLE (76420-898-60)
76420-898-90 76420-898 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20250110 N/A ANDA ANDA203695 Asclemed USA, Inc. METAXALONE 800 mg/1 90 TABLET in 1 BOTTLE (76420-898-90)
68788-7018-0 68788-7018 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20171011 N/A ANDA ANDA203695 Preferred Pharmaceuticals Inc. METAXALONE 800 mg/1 100 TABLET in 1 BOTTLE (68788-7018-0)
68788-7018-1 68788-7018 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20171011 N/A ANDA ANDA203695 Preferred Pharmaceuticals Inc. METAXALONE 800 mg/1 15 TABLET in 1 BOTTLE (68788-7018-1)
68788-7018-2 68788-7018 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20171011 N/A ANDA ANDA203695 Preferred Pharmaceuticals Inc. METAXALONE 800 mg/1 20 TABLET in 1 BOTTLE (68788-7018-2)
68788-7018-3 68788-7018 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20171011 N/A ANDA ANDA203695 Preferred Pharmaceuticals Inc. METAXALONE 800 mg/1 30 TABLET in 1 BOTTLE (68788-7018-3)
68788-7018-6 68788-7018 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20171011 N/A ANDA ANDA203695 Preferred Pharmaceuticals Inc. METAXALONE 800 mg/1 60 TABLET in 1 BOTTLE (68788-7018-6)
76420-898-15 76420-898 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20250110 N/A ANDA ANDA203695 Asclemed USA, Inc. METAXALONE 800 mg/1 15 TABLET in 1 BOTTLE (76420-898-15)
76420-898-12 76420-898 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20250513 N/A ANDA ANDA203695 Asclemed USA, Inc. METAXALONE 800 mg/1 12 TABLET in 1 BOTTLE (76420-898-12)
76420-898-01 76420-898 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20250110 N/A ANDA ANDA203695 Asclemed USA, Inc. METAXALONE 800 mg/1 100 TABLET in 1 BOTTLE (76420-898-01)
80425-0131-2 80425-0131 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20170619 N/A ANDA ANDA203695 Advanced Rx Pharmacy of Tennessee, LLC METAXALONE 800 mg/1 60 TABLET in 1 BOTTLE (80425-0131-2)
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