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"
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
63981-368-79 63981-368 HUMAN OTC DRUG kirkland signature naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20070604 N/A ANDA ANDA074661 Costco Wholesale Company NAPROXEN SODIUM 220 mg/1 400 TABLET, FILM COATED in 1 BOTTLE (63981-368-79)
37808-713-79 37808-713 HUMAN OTC DRUG naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20171003 N/A ANDA ANDA074661 H E B NAPROXEN SODIUM 220 mg/1 400 TABLET, FILM COATED in 1 BOTTLE (37808-713-79)
11673-909-75 11673-909 HUMAN OTC DRUG up and up naproxen sodium naproxen sodium TABLET, FILM COATED ORAL 20220210 N/A ANDA ANDA074661 Target Corporation NAPROXEN SODIUM 220 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (11673-909-75)
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
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
63187-596-24 63187-596 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170901 N/A ANDA ANDA074661 Proficient Rx LP NAPROXEN SODIUM 220 mg/1 24 TABLET, FILM COATED in 1 BOTTLE (63187-596-24)
63187-596-28 63187-596 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170801 N/A ANDA ANDA074661 Proficient Rx LP NAPROXEN SODIUM 220 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (63187-596-28)
63187-596-30 63187-596 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20150803 N/A ANDA ANDA074661 Proficient Rx LP NAPROXEN SODIUM 220 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-596-30)
63187-596-60 63187-596 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20150803 N/A ANDA ANDA074661 Proficient Rx LP NAPROXEN SODIUM 220 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-596-60)
63187-596-90 63187-596 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20150803 N/A ANDA ANDA074661 Proficient Rx LP NAPROXEN SODIUM 220 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-596-90)
72789-543-14 72789-543 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20251223 N/A ANDA ANDA074661 PD-Rx Pharmaceuticals, Inc. NAPROXEN SODIUM 220 mg/1 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-543-14)
72789-543-28 72789-543 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20251223 N/A ANDA ANDA074661 PD-Rx Pharmaceuticals, Inc. NAPROXEN SODIUM 220 mg/1 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-543-28)
41163-511-62 41163-511 HUMAN OTC DRUG equaline naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20140924 N/A ANDA ANDA074661 United Natural Foods, Inc. dba UNFI NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (41163-511-62) / 24 TABLET, FILM COATED in 1 BOTTLE
41163-511-71 41163-511 HUMAN OTC DRUG equaline naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20140924 N/A ANDA ANDA074661 United Natural Foods, Inc. dba UNFI NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (41163-511-71) / 50 TABLET, FILM COATED in 1 BOTTLE
50090-3356-0 50090-3356 HUMAN OTC DRUG rugby all day relief Naproxen Sodium TABLET, FILM COATED ORAL 20180131 N/A ANDA ANDA074661 A-S Medication Solutions NAPROXEN SODIUM 220 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-3356-0)
50090-3356-1 50090-3356 HUMAN OTC DRUG rugby all day relief Naproxen Sodium TABLET, FILM COATED ORAL 20250313 N/A ANDA ANDA074661 A-S Medication Solutions NAPROXEN SODIUM 220 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (50090-3356-1)
71335-1061-1 71335-1061 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20211228 N/A ANDA ANDA074661 Bryant Ranch Prepack NAPROXEN SODIUM 220 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-1061-1)
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