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
85766-121-01 85766-121 HUMAN OTC DRUG Medique Mediproxen NAPROXEN SODIUM TABLET, FILM COATED ORAL 20251217 N/A ANDA ANDA079096 Sportpharm, Inc. dba Sportpharm NAPROXEN SODIUM 220 mg/1 1 TABLET, FILM COATED in 1 PACKET (85766-121-01)
85766-121-10 85766-121 HUMAN OTC DRUG Medique Mediproxen NAPROXEN SODIUM TABLET, FILM COATED ORAL 20251217 N/A ANDA ANDA079096 Sportpharm, Inc. dba Sportpharm NAPROXEN SODIUM 220 mg/1 100 PACKET in 1 BOX (85766-121-10) / 1 TABLET, FILM COATED in 1 PACKET (85766-121-01)
85766-121-50 85766-121 HUMAN OTC DRUG Medique Mediproxen NAPROXEN SODIUM TABLET, FILM COATED ORAL 20251217 N/A ANDA ANDA079096 Sportpharm, Inc. dba Sportpharm NAPROXEN SODIUM 220 mg/1 50 PACKET in 1 BOX (85766-121-50) / 1 TABLET, FILM COATED in 1 PACKET
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
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
68998-144-03 68998-144 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20090601 N/A ANDA ANDA079096 Marc Glassman, Inc. NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (68998-144-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
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
51824-109-01 51824-109 HUMAN OTC DRUG CAREALL Naproxen Sodium Naproxen Sodium TABLET ORAL 20240823 N/A ANDA ANDA079096 New World Imports, Inc. NAPROXEN SODIUM 220 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (51824-109-01)
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
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
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
63941-144-01 63941-144 HUMAN OTC DRUG All Day Pain Relief NAPROXEN SODIUM TABLET, COATED ORAL 20100629 20261031 ANDA ANDA079096 VALU MERCHANDISERS COMPANY NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63941-144-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
63941-144-02 63941-144 HUMAN OTC DRUG All Day Pain Relief NAPROXEN SODIUM TABLET, COATED ORAL 20100610 20261031 ANDA ANDA079096 VALU MERCHANDISERS COMPANY NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63941-144-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
63941-144-03 63941-144 HUMAN OTC DRUG All Day Pain Relief NAPROXEN SODIUM TABLET, COATED ORAL 20100803 20261031 ANDA ANDA079096 VALU MERCHANDISERS COMPANY NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63941-144-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
63868-465-01 63868-465 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20090903 20271231 ANDA ANDA079096 Chain Drug Marketing Association NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63868-465-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
63868-465-50 63868-465 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20090903 20271231 ANDA ANDA079096 Chain Drug Marketing Association NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63868-465-50) / 50 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
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
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