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 3 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
53746-192-08 53746-192 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 8 TABLET in 1 VIAL (53746-192-08)
53746-192-24 53746-192 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 (53746-192-24)
53943-144-02 53943-144 HUMAN OTC DRUG NAPROXEN NAPROXEN SODIUM TABLET, COATED ORAL 20141028 N/A ANDA ANDA079096 DISCOUNT DRUG MART NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (53943-144-02) / 50 TABLET, COATED 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
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
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
59726-169-15 59726-169 HUMAN OTC DRUG All Day Pain Relief Naproxen sodium TABLET ORAL 20140228 N/A ANDA ANDA079096 P & L Development, LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 BOX (59726-169-15) / 15 TABLET in 1 BOTTLE, PLASTIC
59726-169-40 59726-169 HUMAN OTC DRUG All Day Pain Relief Naproxen sodium TABLET ORAL 20140228 N/A ANDA ANDA079096 P & L Development, LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 BOX (59726-169-40) / 40 TABLET 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
63868-466-01 63868-466 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20090619 20280131 ANDA ANDA079096 Chain Drug Marketing Association NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63868-466-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
63868-466-25 63868-466 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20130502 20270930 ANDA ANDA079096 Chain Drug Marketing Association NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63868-466-25) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
63868-466-50 63868-466 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20090619 20270930 ANDA ANDA079096 Chain Drug Marketing Association NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63868-466-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
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
63941-245-01 63941-245 HUMAN OTC DRUG All Day Pain Relief NAPROXEN SODIUM TABLET, COATED ORAL 20100610 20261130 ANDA ANDA079096 VALU MERCHANDISERS COMPANY NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63941-245-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
63941-245-02 63941-245 HUMAN OTC DRUG All Day Pain Relief NAPROXEN SODIUM TABLET, COATED ORAL 20100519 20261130 ANDA ANDA079096 VALU MERCHANDISERS COMPANY NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63941-245-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
63941-245-03 63941-245 HUMAN OTC DRUG All Day Pain Relief NAPROXEN SODIUM TABLET, COATED ORAL 20100519 20270930 ANDA ANDA079096 VALU MERCHANDISERS COMPANY NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63941-245-03) / 100 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
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