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"
符合检索条件的记录共 67 条，共 4 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
42507-844-01 42507-844 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20260113 N/A ANDA ANDA079096 HYVEE INC NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (42507-844-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
42507-844-14 42507-844 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20260113 N/A ANDA ANDA079096 HYVEE INC NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (42507-844-14) / 90 TABLET, COATED in 1 BOTTLE, PLASTIC
50090-2388-0 50090-2388 HUMAN OTC DRUG Medique Mediproxen NAPROXEN SODIUM TABLET, FILM COATED ORAL 20160428 N/A ANDA ANDA079096 A-S Medication Solutions NAPROXEN SODIUM 220 mg/1 100 PACKET in 1 BOX, UNIT-DOSE (50090-2388-0) / 1 TABLET, FILM COATED in 1 PACKET
67091-140-10 67091-140 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20141215 N/A ANDA ANDA079096 WinCo Foods, LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (67091-140-10) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
67091-140-50 67091-140 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20141215 N/A ANDA ANDA079096 WinCo Foods, LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (67091-140-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
67091-138-50 67091-138 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20141215 N/A ANDA ANDA079096 WinCo Foods, LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (67091-138-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
47682-037-50 47682-037 HUMAN OTC DRUG Belmora Flanax Naproxen Sodium TABLET, FILM COATED ORAL 20081230 N/A ANDA ANDA079096 Unifirst First Aid Corporation NAPROXEN SODIUM 220 mg/1 50 PACKET in 1 BOX (47682-037-50) / 1 TABLET, FILM COATED in 1 PACKET
83324-108-01 83324-108 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20250520 N/A ANDA ANDA079096 CHAIN DRUG MARKETING ASSOCIATION, INC. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (83324-108-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
83324-108-24 83324-108 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20250520 N/A ANDA ANDA079096 CHAIN DRUG MARKETING ASSOCIATION, INC. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (83324-108-24) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
47682-237-33 47682-237 HUMAN OTC DRUG Medique Mediproxen NAPROXEN SODIUM TABLET, FILM COATED ORAL 20081230 N/A ANDA ANDA079096 Unifirst First Aid Corporation NAPROXEN SODIUM 220 mg/1 100 PACKET in 1 BOX (47682-237-33) / 1 TABLET, FILM COATED in 1 PACKET (47682-237-46)
83324-109-01 83324-109 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20250520 N/A ANDA ANDA079096 CHAIN DRUG MARKETING ASSOCIATION, INC. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 PACKAGE (83324-109-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
83324-109-50 83324-109 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20250520 N/A ANDA ANDA079096 CHAIN DRUG MARKETING ASSOCIATION, INC. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (83324-109-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
47682-237-46 47682-237 HUMAN OTC DRUG Medique Mediproxen NAPROXEN SODIUM TABLET, FILM COATED ORAL 20081230 N/A ANDA ANDA079096 Unifirst First Aid Corporation NAPROXEN SODIUM 220 mg/1 1 TABLET, FILM COATED in 1 PACKET (47682-237-46)
57344-145-01 57344-145 HUMAN OTC DRUG NAPROXEN SODIUM NAPROXEN SODIUM TABLET, COATED ORAL 20120401 N/A ANDA ANDA079096 AAA Pharmaceutical, Inc. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (57344-145-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
37808-068-24 37808-068 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET ORAL 20150930 N/A ANDA ANDA079096 H E B NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 BOX (37808-068-24) / 24 TABLET in 1 BOTTLE, PLASTIC
37808-068-50 37808-068 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET ORAL 20150930 N/A ANDA ANDA079096 H E B NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 BOX (37808-068-50) / 50 TABLET in 1 BOTTLE, PLASTIC
47682-237-50 47682-237 HUMAN OTC DRUG Medique Mediproxen NAPROXEN SODIUM TABLET, FILM COATED ORAL 20081230 N/A ANDA ANDA079096 Unifirst First Aid Corporation NAPROXEN SODIUM 220 mg/1 50 PACKET in 1 BOX (47682-237-50) / 1 TABLET, FILM COATED in 1 PACKET
47682-737-50 47682-737 HUMAN OTC DRUG Medique at Home Mediproxen Naproxen Sodium TABLET, FILM COATED ORAL 20210201 N/A ANDA ANDA079096 Unifirst First Aid Corporation NAPROXEN SODIUM 220 mg/1 50 PACKET in 1 BOX (47682-737-50) / 1 TABLET, FILM COATED in 1 PACKET (47682-737-46)
83324-108-50 83324-108 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20250520 N/A ANDA ANDA079096 CHAIN DRUG MARKETING ASSOCIATION, INC. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (83324-108-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
53746-191-24 53746-191 HUMAN OTC DRUG Naproxen Sodium (NSAID) Fever Reducer/ Pain Reliever Naproxen Sodium TABLET ORAL 20091125 N/A ANDA ANDA079096 Amneal Pharmaceuticals of New York LLC NAPROXEN SODIUM 220 mg/1 24 TABLET in 1 BOTTLE (53746-191-24)
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