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=ANDA202843"
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
68788-8099-9 68788-8099 HUMAN PRESCRIPTION DRUG Montelukast Montelukast TABLET, FILM COATED ORAL 20211006 N/A ANDA ANDA202843 Preferred Pharmaceuticals, Inc. MONTELUKAST SODIUM 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8099-9)
31722-726-01 31722-726 HUMAN PRESCRIPTION DRUG MONTELUKAST SODIUM MONTELUKAST SODIUM TABLET, FILM COATED ORAL 20140910 N/A ANDA ANDA202843 Camber Pharmaceuticals, Inc. MONTELUKAST SODIUM 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (31722-726-01)
31722-726-10 31722-726 HUMAN PRESCRIPTION DRUG MONTELUKAST SODIUM MONTELUKAST SODIUM TABLET, FILM COATED ORAL 20140910 N/A ANDA ANDA202843 Camber Pharmaceuticals, Inc. MONTELUKAST SODIUM 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (31722-726-10)
31722-726-30 31722-726 HUMAN PRESCRIPTION DRUG MONTELUKAST SODIUM MONTELUKAST SODIUM TABLET, FILM COATED ORAL 20140910 N/A ANDA ANDA202843 Camber Pharmaceuticals, Inc. MONTELUKAST SODIUM 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-726-30)
31722-726-32 31722-726 HUMAN PRESCRIPTION DRUG MONTELUKAST SODIUM MONTELUKAST SODIUM TABLET, FILM COATED ORAL 20140910 N/A ANDA ANDA202843 Camber Pharmaceuticals, Inc. MONTELUKAST SODIUM 10 mg/1 10 BLISTER PACK in 1 CARTON (31722-726-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-726-31)
31722-726-90 31722-726 HUMAN PRESCRIPTION DRUG MONTELUKAST SODIUM MONTELUKAST SODIUM TABLET, FILM COATED ORAL 20140910 N/A ANDA ANDA202843 Camber Pharmaceuticals, Inc. MONTELUKAST SODIUM 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (31722-726-90)
55154-8075-0 55154-8075 HUMAN PRESCRIPTION DRUG Montelukast Sodium Montelukast Sodium TABLET, FILM COATED ORAL 20140910 N/A ANDA ANDA202843 Cardinal Health 107, LLC MONTELUKAST SODIUM 10 mg/1 10 BLISTER PACK in 1 BAG (55154-8075-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
50268-556-15 50268-556 HUMAN PRESCRIPTION DRUG Montelukast Montelukast TABLET, FILM COATED ORAL 20220208 N/A ANDA ANDA202843 AvPAK MONTELUKAST SODIUM 10 mg/1 50 BLISTER PACK in 1 BOX (50268-556-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-556-11)
50090-6109-0 50090-6109 HUMAN PRESCRIPTION DRUG Montelukast Montelukast TABLET, FILM COATED ORAL 20220928 N/A ANDA ANDA202843 A-S Medication Solutions MONTELUKAST SODIUM 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6109-0)
82009-009-10 82009-009 HUMAN PRESCRIPTION DRUG Montelukast Montelukast TABLET, FILM COATED ORAL 20220607 N/A ANDA ANDA202843 Quallent Pharmaceuticals Health LLC MONTELUKAST SODIUM 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (82009-009-10)
71610-563-30 71610-563 HUMAN PRESCRIPTION DRUG Montelukast Montelukast TABLET, FILM COATED ORAL 20210527 N/A ANDA ANDA202843 Aphena Pharma Solutions - Tennessee, LLC MONTELUKAST SODIUM 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71610-563-30)
72865-175-10 72865-175 HUMAN PRESCRIPTION DRUG Montelukast Montelukast TABLET, FILM COATED ORAL 20210211 N/A ANDA ANDA202843 XLCare Pharmaceuticals Inc. MONTELUKAST SODIUM 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (72865-175-10)
72865-175-30 72865-175 HUMAN PRESCRIPTION DRUG Montelukast Montelukast TABLET, FILM COATED ORAL 20210211 N/A ANDA ANDA202843 XLCare Pharmaceuticals Inc. MONTELUKAST SODIUM 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72865-175-30)
72865-175-90 72865-175 HUMAN PRESCRIPTION DRUG Montelukast Montelukast TABLET, FILM COATED ORAL 20210211 N/A ANDA ANDA202843 XLCare Pharmaceuticals Inc. MONTELUKAST SODIUM 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72865-175-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase