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=ANDA079096"
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
63941-444-02 63941-444 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20240501 N/A ANDA ANDA079096 VALU MERCHANDISERS COMPANY NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63941-444-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
63941-444-03 63941-444 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20240501 N/A ANDA ANDA079096 VALU MERCHANDISERS COMPANY NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63941-444-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
63941-445-01 63941-445 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20240501 N/A ANDA ANDA079096 VALU MERCHANDISERS COMPANY NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63941-445-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
81522-045-05 81522-045 HUMAN OTC DRUG NAPROXEN SODIUM NAPROXEN SODIUM TABLET, COATED ORAL 20230502 N/A ANDA ANDA079096 FSA STORE INC. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (81522-045-05) / 200 TABLET, COATED in 1 BOTTLE, PLASTIC
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase