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=ANDA074661"
符合检索条件的记录共 132 条，共 7 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
55910-481-62 55910-481 HUMAN OTC DRUG DG Health Naproxen Sodium naproxen sodium TABLET, FILM COATED ORAL 20210526 N/A ANDA ANDA074661 Dolgencorp Inc NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (55910-481-62) / 24 TABLET, FILM COATED in 1 BOTTLE
55910-481-71 55910-481 HUMAN OTC DRUG DG Health Naproxen Sodium naproxen sodium TABLET, FILM COATED ORAL 20210526 N/A ANDA ANDA074661 Dolgencorp Inc NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (55910-481-71) / 50 TABLET, FILM COATED in 1 BOTTLE
55910-490-62 55910-490 HUMAN OTC DRUG DG Health Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20160425 N/A ANDA ANDA074661 Dolgencorp Inc NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (55910-490-62) / 24 TABLET, FILM COATED in 1 BOTTLE
55910-500-82 55910-500 HUMAN OTC DRUG dg health naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170905 N/A ANDA ANDA074661 Dolgencorp Inc NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (55910-500-82) / 200 TABLET, FILM COATED in 1 BOTTLE
80267-001-71 80267-001 HUMAN OTC DRUG betr headache pain relief naproxen sodium TABLET, FILM COATED ORAL 20210209 N/A ANDA ANDA074661 Live Betr LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (80267-001-71) / 50 TABLET, FILM COATED in 1 BOTTLE
0113-0901-62 0113-0901 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20140423 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0113-0901-62) / 24 TABLET, FILM COATED in 1 BOTTLE
0113-0901-71 0113-0901 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20140423 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0113-0901-71) / 50 TABLET, FILM COATED in 1 BOTTLE
0113-0901-75 0113-0901 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20211208 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0113-0901-75) / 90 TABLET, FILM COATED in 1 BOTTLE
0113-1412-71 0113-1412 HUMAN OTC DRUG good sense naproxen sodium naproxen sodium TABLET, FILM COATED ORAL 20211109 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0113-1412-71) / 50 TABLET, FILM COATED in 1 BOTTLE
0113-4368-62 0113-4368 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20140331 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0113-4368-62) / 24 TABLET, FILM COATED in 1 BOTTLE
0113-4368-71 0113-4368 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20140331 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0113-4368-71) / 50 TABLET, FILM COATED in 1 BOTTLE
0113-4368-75 0113-4368 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20211208 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0113-4368-75) / 90 TABLET, FILM COATED in 1 BOTTLE
0113-4368-79 0113-4368 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20180619 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 400 TABLET, FILM COATED in 1 BOTTLE (0113-4368-79)
59779-914-75 59779-914 HUMAN OTC DRUG naproxen sodium Naproxen sodium TABLET, FILM COATED ORAL 20220307 N/A ANDA ANDA074661 CVS Pharmacy NAPROXEN SODIUM 220 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (59779-914-75)
41250-818-62 41250-818 HUMAN OTC DRUG naproxen sodium naproxen sodium TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA074661 Meijer Distribution Inc NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (41250-818-62) / 24 TABLET, FILM COATED in 1 BOTTLE
41250-818-75 41250-818 HUMAN OTC DRUG naproxen sodium naproxen sodium TABLET, FILM COATED ORAL 20220602 N/A ANDA ANDA074661 Meijer Distribution Inc NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (41250-818-75) / 90 TABLET, FILM COATED in 1 BOTTLE
0363-0938-82 0363-0938 HUMAN OTC DRUG all day pain relief Naproxen Sodium TABLET, FILM COATED ORAL 20140731 N/A ANDA ANDA074661 Walgreen Company NAPROXEN SODIUM 200 mg/1 200 TABLET, FILM COATED in 1 BOTTLE (0363-0938-82)
0536-1093-06 0536-1093 HUMAN OTC DRUG Rugby All Day Relief Naproxen Sodium TABLET, FILM COATED ORAL 20150915 N/A ANDA ANDA074661 Rugby Laboratories NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0536-1093-06) / 50 TABLET, FILM COATED in 1 BOTTLE
0536-1093-11 0536-1093 HUMAN OTC DRUG Rugby All Day Relief Naproxen Sodium TABLET, FILM COATED ORAL 20220318 N/A ANDA ANDA074661 Rugby Laboratories NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0536-1093-11) / 90 TABLET, FILM COATED in 1 BOTTLE
0536-1094-06 0536-1094 HUMAN OTC DRUG rugby all day relief Naproxen Sodium TABLET, FILM COATED ORAL 20150902 N/A ANDA ANDA074661 Rugby Laboratories NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0536-1094-06) / 50 TABLET, FILM COATED in 1 BOTTLE
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