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"
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
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)
71335-1282-4 71335-1282 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20250110 N/A ANDA ANDA204872 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 50 TABLET in 1 BOTTLE (71335-1282-4)
71335-1282-5 71335-1282 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20250130 N/A ANDA ANDA204872 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 60 TABLET in 1 BOTTLE (71335-1282-5)
71335-1282-6 71335-1282 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20191126 N/A ANDA ANDA204872 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 14 TABLET in 1 BOTTLE (71335-1282-6)
71335-1282-7 71335-1282 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20191025 N/A ANDA ANDA204872 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 100 TABLET in 1 BOTTLE (71335-1282-7)
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)
57896-954-05 57896-954 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20190101 N/A ANDA ANDA204872 Geri-Care Pharmaceutical Corp NAPROXEN SODIUM 220 mg/1 50 TABLET in 1 BOTTLE (57896-954-05)
71335-1282-9 71335-1282 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20250130 N/A ANDA ANDA204872 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 24 TABLET in 1 BOTTLE (71335-1282-9)
71335-1282-8 71335-1282 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20250130 N/A ANDA ANDA204872 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 90 TABLET in 1 BOTTLE (71335-1282-8)
57896-954-01 57896-954 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20190101 N/A ANDA ANDA204872 Geri-Care Pharmaceutical Corp NAPROXEN SODIUM 220 mg/1 100 TABLET in 1 BOTTLE (57896-954-01)
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)
68788-7572-2 68788-7572 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20191227 N/A ANDA ANDA204872 Preferred Pharmaceuticals, Inc. NAPROXEN SODIUM 220 mg/1 20 TABLET in 1 BOTTLE (68788-7572-2)
68788-7572-3 68788-7572 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20191227 N/A ANDA ANDA204872 Preferred Pharmaceuticals, Inc. NAPROXEN SODIUM 220 mg/1 30 TABLET in 1 BOTTLE (68788-7572-3)
68788-7572-4 68788-7572 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20191227 N/A ANDA ANDA204872 Preferred Pharmaceuticals, Inc. NAPROXEN SODIUM 220 mg/1 40 TABLET in 1 BOTTLE (68788-7572-4)
71205-595-24 71205-595 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20230728 N/A ANDA ANDA204872 Proficient Rx LP NAPROXEN SODIUM 220 mg/1 24 TABLET in 1 BOTTLE (71205-595-24)
71205-595-30 71205-595 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20210727 N/A ANDA ANDA204872 Proficient Rx LP NAPROXEN SODIUM 220 mg/1 30 TABLET in 1 BOTTLE (71205-595-30)
71205-595-60 71205-595 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20210727 N/A ANDA ANDA204872 Proficient Rx LP NAPROXEN SODIUM 220 mg/1 60 TABLET in 1 BOTTLE (71205-595-60)
71205-595-90 71205-595 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20210727 N/A ANDA ANDA204872 Proficient Rx LP NAPROXEN SODIUM 220 mg/1 90 TABLET in 1 BOTTLE (71205-595-90)
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
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