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 62 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
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
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
63941-144-01 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
63941-144-03 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
63941-245-02 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
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
63941-444-02 63941-444 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20240501 N/A ANDA ANDA079096 VALU MERCHANDISERS COMPANY NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63941-444-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
63941-445-02 63941-445 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20240501 N/A ANDA ANDA079096 VALU MERCHANDISERS COMPANY NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63941-445-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
63941-445-03 63941-445 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20240501 N/A ANDA ANDA079096 VALU MERCHANDISERS COMPANY NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63941-445-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
63941-444-03 63941-444 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20240501 N/A ANDA ANDA079096 VALU MERCHANDISERS COMPANY NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63941-444-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
63941-444-01 63941-444 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20240501 N/A ANDA ANDA079096 VALU MERCHANDISERS COMPANY NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63941-444-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
63941-445-01 63941-445 HUMAN OTC DRUG Naproxen Sodium NAPROXEN SODIUM TABLET, COATED ORAL 20240501 N/A ANDA ANDA079096 VALU MERCHANDISERS COMPANY NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 CARTON (63941-445-01) / 24 TABLET, COATED 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
33992-0169-4 33992-0169 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET ORAL 20200313 20251231 ANDA ANDA079096 ASSURED / DOLLAR TREE (Greenbrier International, Inc.) NAPROXEN SODIUM 220 mg/1 1 BOTTLE, PLASTIC in 1 BOX (33992-0169-4) / 24 TABLET 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
83324-109-50 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
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
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