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 131 条，共 7 页，当前第 5 页 ，可点击列名称排序
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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
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)
36800-140-82 36800-140 HUMAN OTC DRUG Topcare All Day Pain Relief Naproxen sodium TABLET, FILM COATED ORAL 20071203 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 200 TABLET, FILM COATED in 1 BOTTLE (36800-140-82)
36800-368-76 36800-368 HUMAN OTC DRUG TopCare All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20070629 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-368-76) / 120 TABLET, FILM COATED in 1 BOTTLE
36800-368-82 36800-368 HUMAN OTC DRUG TopCare All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20040127 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-368-82) / 200 TABLET, FILM COATED in 1 BOTTLE
36800-368-62 36800-368 HUMAN OTC DRUG TopCare All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 19970722 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-368-62) / 24 TABLET, FILM COATED in 1 BOTTLE
36800-368-71 36800-368 HUMAN OTC DRUG TopCare All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 19970114 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-368-71) / 50 TABLET, FILM COATED in 1 BOTTLE
36800-368-75 36800-368 HUMAN OTC DRUG TopCare All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20220712 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-368-75) / 90 TABLET, FILM COATED in 1 BOTTLE
21130-180-79 21130-180 HUMAN OTC DRUG signature care naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20211123 20270228 ANDA ANDA074661 Safeway NAPROXEN SODIUM 220 mg/1 400 TABLET, FILM COATED in 1 BOTTLE (21130-180-79)
36800-490-62 36800-490 HUMAN OTC DRUG Topcare All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 19970722 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-490-62) / 24 TABLET, FILM COATED in 1 BOTTLE
36800-490-71 36800-490 HUMAN OTC DRUG Topcare All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 19970114 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-490-71) / 50 TABLET, FILM COATED in 1 BOTTLE
36800-490-75 36800-490 HUMAN OTC DRUG Topcare All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20211209 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-490-75) / 90 TABLET, FILM COATED in 1 BOTTLE
45802-490-75 45802-490 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20211202 N/A ANDA ANDA074661 Padagis Israel Pharmaceuticals Ltd NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (45802-490-75) / 90 TABLET, FILM COATED in 1 BOTTLE
36800-696-75 36800-696 HUMAN OTC DRUG topcare back and muscle pain naproxen sodium TABLET, FILM COATED ORAL 20211213 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-696-75) / 90 TABLET, FILM COATED in 1 BOTTLE
21130-593-79 21130-593 HUMAN OTC DRUG NAPROXEN SODIUM Naproxen Sodium TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA074661 Safeway NAPROXEN SODIUM 220 mg/1 400 TABLET, FILM COATED in 1 BOTTLE (21130-593-79)
41250-313-82 41250-313 HUMAN OTC DRUG naproxen sodium Naproxen sodium TABLET, FILM COATED ORAL 20040528 N/A ANDA ANDA074661 Meijer Distribution Inc NAPROXEN SODIUM 220 mg/1 200 TABLET, FILM COATED in 1 BOTTLE (41250-313-82)
68788-8443-2 68788-8443 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA074661 Preferred Pharmaceuticals Inc. NAPROXEN SODIUM 220 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68788-8443-2)
68788-8443-3 68788-8443 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA074661 Preferred Pharmaceuticals Inc. NAPROXEN SODIUM 220 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8443-3)
68788-8443-4 68788-8443 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA074661 Preferred Pharmaceuticals Inc. NAPROXEN SODIUM 220 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (68788-8443-4)
68788-8443-6 68788-8443 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA074661 Preferred Pharmaceuticals Inc. NAPROXEN SODIUM 220 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8443-6)
41250-477-62 41250-477 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20180706 N/A ANDA ANDA074661 Meijer Distribution Inc NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (41250-477-62) / 24 TABLET, FILM COATED in 1 BOTTLE
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