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
68788-7572-2 68788-7572 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20191227 N/A ANDA ANDA204872 Preferred Pharmaceuticals, Inc. NAPROXEN SODIUM 220 mg/1 20 TABLET in 1 BOTTLE (68788-7572-2)
68788-7572-3 68788-7572 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20191227 N/A ANDA ANDA204872 Preferred Pharmaceuticals, Inc. NAPROXEN SODIUM 220 mg/1 30 TABLET in 1 BOTTLE (68788-7572-3)
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
68788-7572-4 68788-7572 HUMAN OTC DRUG Naproxen Naproxen Sodium TABLET ORAL 20191227 N/A ANDA ANDA204872 Preferred Pharmaceuticals, Inc. NAPROXEN SODIUM 220 mg/1 40 TABLET in 1 BOTTLE (68788-7572-4)
27854-170-01 27854-170 HUMAN OTC DRUG AnaDent Naproxen Sodium TABLET, FILM COATED ORAL 20170123 N/A ANDA ANDA204872 Belmora LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (27854-170-01) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
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
79903-005-20 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 N/A ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-20)
79903-005-27 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 N/A ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-27)
79903-005-30 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 N/A ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-30)
79903-005-75 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 N/A ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (79903-005-75) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
79903-005-90 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 N/A ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-90)
79903-005-99 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 N/A ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-99)
27854-160-01 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 (27854-160-01) / 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
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
79903-005-25 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 N/A ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-25)
79903-005-10 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 N/A ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (79903-005-10) / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
79903-005-12 79903-005 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20201022 N/A ANDA ANDA204872 WALMART INC. NAPROXEN SODIUM 220 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-12)
51316-817-08 51316-817 HUMAN OTC DRUG Back and Muscle Pain Naproxen Sodium TABLET, FILM COATED ORAL 20220418 N/A ANDA ANDA204872 CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (51316-817-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
51316-817-52 51316-817 HUMAN OTC DRUG Back and Muscle Pain Naproxen Sodium TABLET, FILM COATED ORAL 20220418 N/A ANDA ANDA204872 CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (51316-817-52) / 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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