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 95 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
50844-604-98 50844-604 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 (50844-604-98)
50844-604-99 50844-604 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 (50844-604-99)
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)
42961-122-02 42961-122 HUMAN OTC DRUG First Aid Direct All Day Pain Relief Naproxen Sodium TABLET, COATED ORAL 20230719 N/A ANDA ANDA204872 Cintas Corporation NAPROXEN SODIUM 220 mg/1 25 PACKET in 1 BOX (42961-122-02) / 1 TABLET, COATED in 1 PACKET (42961-122-01)
11822-4170-5 11822-4170 HUMAN OTC DRUG Back and Muscle Pain Naproxen Sodium TABLET, FILM COATED ORAL 20220707 N/A ANDA ANDA204872 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (11822-4170-5) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
11822-4171-2 11822-4171 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220707 20250213 ANDA ANDA204872 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (11822-4171-2) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
11822-4171-5 11822-4171 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220707 N/A ANDA ANDA204872 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (11822-4171-5) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
21130-674-52 21130-674 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET, FILM COATED ORAL 20231004 N/A ANDA ANDA204872 Better Living Brands, LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (21130-674-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
11822-6040-8 11822-6040 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220718 N/A ANDA ANDA204872 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-8) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
11822-6040-9 11822-6040 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220718 N/A ANDA ANDA204872 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-9) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
11822-6040-2 11822-6040 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220718 20250103 ANDA ANDA204872 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-2) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
11822-6040-5 11822-6040 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220718 N/A ANDA ANDA204872 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-5) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
11822-6040-6 11822-6040 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220718 N/A ANDA ANDA204872 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-6) / 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
11822-6040-7 11822-6040 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220718 N/A ANDA ANDA204872 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (11822-6040-7)
21130-856-52 21130-856 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20231011 N/A ANDA ANDA204872 Better Living Brands, LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (21130-856-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase