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
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)
68788-8443-3 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)
68788-8443-2 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)
41520-533-71 41520-533 HUMAN OTC DRUG Care One Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20160708 N/A ANDA ANDA074661 American Sales Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (41520-533-71) / 50 TABLET, FILM COATED in 1 BOTTLE
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
69842-811-62 69842-811 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20180509 N/A ANDA ANDA074661 CVS Pharmacy NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (69842-811-62) / 24 TABLET, FILM COATED in 1 BOTTLE
69842-811-71 69842-811 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20180509 N/A ANDA ANDA074661 CVS Pharmacy NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (69842-811-71) / 50 TABLET, FILM COATED in 1 BOTTLE
69842-811-75 69842-811 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220408 N/A ANDA ANDA074661 CVS Pharmacy NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (69842-811-75) / 90 TABLET, FILM COATED in 1 BOTTLE
69842-811-90 69842-811 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20180509 N/A ANDA ANDA074661 CVS Pharmacy NAPROXEN SODIUM 220 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (69842-811-90)
41520-349-82 41520-349 HUMAN OTC DRUG Care One Naproxen Sodium Naproxen sodium TABLET, FILM COATED ORAL 20160613 N/A ANDA ANDA074661 American Sales Company NAPROXEN SODIUM 220 mg/1 200 TABLET, FILM COATED in 1 BOTTLE (41520-349-82)
41520-507-71 41520-507 HUMAN OTC DRUG CareOne Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20160805 N/A ANDA ANDA074661 American Sales Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (41520-507-71) / 50 TABLET, FILM COATED in 1 BOTTLE
41520-507-75 41520-507 HUMAN OTC DRUG CareOne Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220225 N/A ANDA ANDA074661 American Sales Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (41520-507-75) / 90 TABLET, FILM COATED in 1 BOTTLE
41520-507-87 41520-507 HUMAN OTC DRUG CareOne Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20180525 N/A ANDA ANDA074661 American Sales Company NAPROXEN SODIUM 220 mg/1 300 TABLET, FILM COATED in 1 BOTTLE (41520-507-87)
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