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=ANDA205497"
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
58602-737-38 58602-737 HUMAN OTC DRUG Naproxen Sodium HEADACHE PAIN Naproxen Sodium TABLET, FILM COATED ORAL 20210714 N/A ANDA ANDA205497 Aurohealth LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (58602-737-38) / 300 TABLET, FILM COATED in 1 BOTTLE
58602-737-40 58602-737 HUMAN OTC DRUG Naproxen Sodium HEADACHE PAIN Naproxen Sodium TABLET, FILM COATED ORAL 20210714 N/A ANDA ANDA205497 Aurohealth LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (58602-737-40) / 500 TABLET, FILM COATED in 1 BOTTLE
58602-737-44 58602-737 HUMAN OTC DRUG Naproxen Sodium HEADACHE PAIN Naproxen Sodium TABLET, FILM COATED ORAL 20210714 N/A ANDA ANDA205497 Aurohealth LLC NAPROXEN SODIUM 220 mg/1 400 TABLET, FILM COATED in 1 BOTTLE (58602-737-44)
58602-737-78 58602-737 HUMAN OTC DRUG Naproxen Sodium HEADACHE PAIN Naproxen Sodium TABLET, FILM COATED ORAL 20210714 N/A ANDA ANDA205497 Aurohealth LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (58602-737-78) / 50 TABLET, FILM COATED in 1 BOTTLE
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