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"
符合检索条件的记录共 90 条，共 5 页，当前第 4 页 ，可点击列名称排序
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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
50844-417-16 50844-417 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-16)
50844-417-19 50844-417 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (50844-417-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50844-417-22 50844-417 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 48 POUCH in 1 CARTON (50844-417-22) / 1 TABLET, FILM COATED in 1 POUCH (50844-417-43)
50844-417-56 50844-417 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-56)
50844-417-98 50844-417 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-98)
50844-417-99 50844-417 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-99)
50844-471-11 50844-471 HUMAN OTC DRUG Naproxen Headache Pain Naproxen Sodium TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 60 POUCH in 1 CARTON (50844-471-11) / 1 TABLET, FILM COATED in 1 POUCH (50844-471-43)
50844-471-14 50844-471 HUMAN OTC DRUG Naproxen Headache Pain Naproxen Sodium TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-14)
50844-471-16 50844-471 HUMAN OTC DRUG Naproxen Headache Pain Naproxen Sodium TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-16)
50844-471-19 50844-471 HUMAN OTC DRUG Naproxen Headache Pain Naproxen Sodium TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (50844-471-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50844-471-22 50844-471 HUMAN OTC DRUG Naproxen Headache Pain Naproxen Sodium TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 48 POUCH in 1 CARTON (50844-471-22) / 1 TABLET, FILM COATED in 1 POUCH (50844-471-43)
50844-471-56 50844-471 HUMAN OTC DRUG Naproxen Headache Pain Naproxen Sodium TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-56)
50844-471-98 50844-471 HUMAN OTC DRUG Naproxen Headache Pain Naproxen Sodium TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-98)
50844-471-99 50844-471 HUMAN OTC DRUG Naproxen Headache Pain Naproxen Sodium TABLET, FILM COATED ORAL 20200916 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-471-99)
50844-604-09 50844-604 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 4 BLISTER PACK in 1 CARTON (50844-604-09) / 5 TABLET, FILM COATED in 1 BLISTER PACK
50844-604-14 50844-604 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-14)
50844-604-15 50844-604 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (50844-604-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50844-604-16 50844-604 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-16)
50844-604-19 50844-604 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (50844-604-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
50844-604-56 50844-604 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-56)
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