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 90 条，共 5 页，当前第 2 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
51316-817-52 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
66715-5428-4 66715-5428 HUMAN OTC DRUG 24/7 Life by 7-Eleven Naproxen Sodium naproxen sodium tablet, film coated TABLET, FILM COATED ORAL 20220419 N/A ANDA ANDA204872 Lil' Drug Store Products, Inc. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (66715-5428-4) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
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
11822-4171-5 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
79903-005-10 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 20260228 ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (79903-005-10) / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
79903-005-12 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 20260228 ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-12)
79903-005-20 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 N/A ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-20)
79903-005-25 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 N/A ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-25)
79903-005-27 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 N/A ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-27)
79903-005-30 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 20260131 ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-30)
79903-005-90 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 N/A ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-90)
79903-005-99 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 20260228 ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-99)
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)
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
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
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase