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=ANDA207466"
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
68788-8678-1 68788-8678 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20240528 N/A ANDA ANDA207466 Preferred Pharmaceuticals Inc. METAXALONE 800 mg/1 100 TABLET in 1 BOTTLE (68788-8678-1)
70518-4559-0 70518-4559 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20260201 N/A ANDA ANDA207466 REMEDYREPACK INC. METAXALONE 800 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (70518-4559-0)
68788-8678-9 68788-8678 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20240528 N/A ANDA ANDA207466 Preferred Pharmaceuticals Inc. METAXALONE 800 mg/1 90 TABLET in 1 BOTTLE (68788-8678-9)
0904-6831-06 0904-6831 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20170831 N/A ANDA ANDA207466 Major Pharmaceuticals METAXALONE 800 mg/1 50 BLISTER PACK in 1 CARTON (0904-6831-06) / 1 TABLET in 1 BLISTER PACK
0276-0508-10 0276-0508 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20211101 N/A ANDA ANDA207466 Misemer Pharmaceuticals, Inc. METAXALONE 400 mg/1 100 TABLET in 1 BOTTLE (0276-0508-10)
0904-6831-04 0904-6831 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20170831 N/A ANDA ANDA207466 Major Pharmaceuticals METAXALONE 800 mg/1 30 BLISTER PACK in 1 CARTON (0904-6831-04) / 1 TABLET in 1 BLISTER PACK
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