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 85 条，共 5 页，当前第 2 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
71205-595-60 71205-595 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20210727 N/A ANDA ANDA204872 Proficient Rx LP NAPROXEN SODIUM 220 mg/1 60 TABLET in 1 BOTTLE (71205-595-60)
71205-595-90 71205-595 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20210727 N/A ANDA ANDA204872 Proficient Rx LP NAPROXEN SODIUM 220 mg/1 90 TABLET in 1 BOTTLE (71205-595-90)
50844-417-11 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 60 POUCH in 1 CARTON (50844-417-11) / 1 TABLET, FILM COATED in 1 POUCH (50844-417-43)
50844-417-14 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/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-14)
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
27854-165-10 27854-165 HUMAN OTC DRUG Flanax Menstrual Pain Reliever Naproxen Sodium TABLET, FILM COATED ORAL 20170123 N/A ANDA ANDA204872 Belmora LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (27854-165-10) / 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
59428-604-08 59428-604 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 N/A ANDA ANDA204872 Zapotol Products Corp NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (59428-604-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
68071-5039-1 68071-5039 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20230110 N/A ANDA ANDA204872 NuCare Pharmaceuticals,Inc. NAPROXEN SODIUM 220 mg/1 21 TABLET in 1 BOTTLE (68071-5039-1)
50844-604-06 50844-604 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20260219 N/A ANDA ANDA204872 L.N.K. International, Inc. NAPROXEN SODIUM 220 mg/1 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-06)
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)
50844-604-98 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 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-98)
50844-604-99 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 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-99)
21130-856-52 21130-856 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20231011 N/A ANDA ANDA204872 Better Living Brands, LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (21130-856-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
55319-406-15 55319-406 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET, FILM COATED ORAL 20231215 N/A ANDA ANDA204872 Family Dollar Services Inc NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (55319-406-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
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