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=ANDA204872"
符合检索条件的记录共 85 条，共 5 页，当前第 3 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
51316-817-08 51316-817 HUMAN OTC DRUG Back and Muscle Pain Naproxen Sodium TABLET, FILM COATED ORAL 20220418 N/A ANDA ANDA204872 CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (51316-817-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
51316-817-52 51316-817 HUMAN OTC DRUG Back and Muscle Pain Naproxen Sodium TABLET, FILM COATED ORAL 20220418 N/A ANDA ANDA204872 CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (51316-817-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
71335-1282-1 71335-1282 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20211118 N/A ANDA ANDA204872 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 20 TABLET in 1 BOTTLE (71335-1282-1)
71335-1282-2 71335-1282 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20190827 N/A ANDA ANDA204872 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 30 TABLET in 1 BOTTLE (71335-1282-2)
71335-1282-3 71335-1282 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20191022 N/A ANDA ANDA204872 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 40 TABLET in 1 BOTTLE (71335-1282-3)
50844-714-14 50844-714 HUMAN OTC DRUG Naproxen Back and Muscle Pain Naproxen Sodium TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-14)
50844-714-16 50844-714 HUMAN OTC DRUG Naproxen Back and Muscle Pain Naproxen Sodium TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-16)
50844-714-19 50844-714 HUMAN OTC DRUG Naproxen Back and Muscle Pain Naproxen Sodium TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (50844-714-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50844-714-56 50844-714 HUMAN OTC DRUG Naproxen Back and Muscle Pain Naproxen Sodium TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-56)
50844-714-98 50844-714 HUMAN OTC DRUG Naproxen Back and Muscle Pain Naproxen Sodium TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-98)
50844-714-99 50844-714 HUMAN OTC DRUG Naproxen Back and Muscle Pain Naproxen Sodium TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-99)
68788-7572-6 68788-7572 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20191227 N/A ANDA ANDA204872 Preferred Pharmaceuticals, Inc. NAPROXEN SODIUM 220 mg/1 60 TABLET in 1 BOTTLE (68788-7572-6)
53185-604-12 53185-604 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220311 N/A ANDA ANDA204872 Athlete's Needs Inc NAPROXEN SODIUM 220 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53185-604-12)
50844-417-11 50844-417 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 60 POUCH in 1 CARTON (50844-417-11) / 1 TABLET, FILM COATED in 1 POUCH (50844-417-43)
50844-417-14 50844-417 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-14)
50844-417-16 50844-417 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-16)
50844-417-19 50844-417 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (50844-417-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50844-417-22 50844-417 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 48 POUCH in 1 CARTON (50844-417-22) / 1 TABLET, FILM COATED in 1 POUCH (50844-417-43)
50844-417-56 50844-417 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-56)
50844-417-98 50844-417 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-98)
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