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=ANDA204872"
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
27854-160-24 27854-160 HUMAN OTC DRUG Flanax Naproxen Sodium TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA204872 Belmora LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (27854-160-24) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
42961-122-02 42961-122 HUMAN OTC DRUG First Aid Direct All Day Pain Relief Naproxen Sodium TABLET, COATED ORAL 20230719 N/A ANDA ANDA204872 Cintas Corporation NAPROXEN SODIUM 220 mg/1 25 PACKET in 1 BOX (42961-122-02) / 1 TABLET, COATED in 1 PACKET (42961-122-01)
46122-564-81 46122-564 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA204872 Amerisource Bergen NAPROXEN SODIUM 220 mg/1 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (46122-564-81)
55319-717-08 55319-717 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET, FILM COATED ORAL 20231213 N/A ANDA ANDA204872 Family Dollar Services Inc NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (55319-717-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
53185-604-15 53185-604 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220311 N/A ANDA ANDA204872 Athlete's Needs Inc NAPROXEN SODIUM 220 mg/1 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53185-604-15)
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