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=ANDA090545"
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
51316-608-90 51316-608 HUMAN OTC DRUG Naproxen Sodium Naproxen sodium 220mg TABLET ORAL 20250501 N/A ANDA ANDA090545 CVS Pharmacy, Inc. NAPROXEN SODIUM 220 mg/1 90 TABLET in 1 BOTTLE (51316-608-90)
48201-007-24 48201-007 HUMAN OTC DRUG CALMADOL PAIN RELIEVER Naproxen Sodium TABLET ORAL 20150331 N/A ANDA ANDA090545 GRANDALL DISTRIBUTING, LLC NAPROXEN SODIUM 220 mg/1 1 PACKET in 1 BOX (48201-007-24) / 24 TABLET in 1 PACKET
27854-505-01 27854-505 HUMAN OTC DRUG Flanax Pain Reliever/Fever reducer Naproxen Sodium TABLET, COATED ORAL 20200515 N/A ANDA ANDA090545 Belmora LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (27854-505-01) / 24 TABLET, COATED in 1 BOTTLE
27854-505-02 27854-505 HUMAN OTC DRUG Flanax Pain Reliever/Fever reducer Naproxen Sodium TABLET, COATED ORAL 20200515 N/A ANDA ANDA090545 Belmora LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (27854-505-02) / 2 TABLET, COATED in 1 BOTTLE
69197-394-24 69197-394 HUMAN OTC DRUG Naproxen Sodium 220mg Naproxen Sodium 220mg TABLET, COATED ORAL 20141223 N/A ANDA ANDA090545 Command Brands, LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (69197-394-24) / 24 TABLET, COATED in 1 BOTTLE
69168-362-07 69168-362 HUMAN OTC DRUG Naproxen Caplets All day relief for pain Naproxen Sodium 220 mg TABLET ORAL 20141223 N/A ANDA ANDA090545 Allegiant Health NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (69168-362-07) / 10 TABLET in 1 BOTTLE
79903-609-09 79903-609 HUMAN OTC DRUG All Day Back and Muscle Pain Relief Naproxen sodium TABLET, COATED ORAL 20231215 N/A ANDA ANDA090545 Walmart Inc. NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (79903-609-09) / 90 TABLET, COATED in 1 BOTTLE
79903-609-20 79903-609 HUMAN OTC DRUG All Day Back and Muscle Pain Relief Naproxen sodium TABLET, COATED ORAL 20231215 N/A ANDA ANDA090545 Walmart Inc. NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (79903-609-20) / 200 TABLET, COATED in 1 BOTTLE
41226-609-05 41226-609 HUMAN OTC DRUG NAPROXEN SODIUM NAPROXEN SODIUM TABLET, COATED ORAL 20210612 N/A ANDA ANDA090545 Kroger Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (41226-609-05) / 50 TABLET, COATED in 1 BOTTLE
25000-141-30 25000-141 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium, Coated Tablets TABLET ORAL 20110528 N/A ANDA ANDA090545 MARKSANS PHARMA LIMITED NAPROXEN SODIUM 220 mg/1 6 BAG in 1 BOX (25000-141-30) / 6500 TABLET in 1 BAG
25000-141-43 25000-141 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium, Coated Tablets TABLET ORAL 20110528 N/A ANDA ANDA090545 MARKSANS PHARMA LIMITED NAPROXEN SODIUM 220 mg/1 10 TABLET in 1 BOTTLE (25000-141-43)
25000-141-98 25000-141 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium, Coated Tablets TABLET ORAL 20110528 N/A ANDA ANDA090545 MARKSANS PHARMA LIMITED NAPROXEN SODIUM 220 mg/1 1 BAG in 1 BOX (25000-141-98) / 32165 TABLET in 1 BAG
21130-608-05 21130-608 HUMAN OTC DRUG Pain Relief Naproxen sodium TABLET ORAL 20230613 N/A ANDA ANDA090545 BETTER LIVING BRANDS, LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (21130-608-05) / 50 TABLET in 1 BOTTLE
21130-608-20 21130-608 HUMAN OTC DRUG Pain Relief Naproxen sodium TABLET ORAL 20230613 N/A ANDA ANDA090545 BETTER LIVING BRANDS, LLC NAPROXEN SODIUM 220 mg/1 200 TABLET in 1 BOTTLE (21130-608-20)
21130-608-42 21130-608 HUMAN OTC DRUG Pain Relief Naproxen sodium TABLET ORAL 20230613 N/A ANDA ANDA090545 BETTER LIVING BRANDS, LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (21130-608-42) / 24 TABLET in 1 BOTTLE
85828-394-92 85828-394 HUMAN OTC DRUG Naproxen Sodium 220mg Naproxen Sodium 220mg TABLET, FILM COATED ORAL 20260318 N/A ANDA ANDA090545 Grocery Outlet NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (85828-394-92) / 90 TABLET, FILM COATED in 1 BOTTLE
53329-688-30 53329-688 HUMAN OTC DRUG Naproxen Sodium 220mg Naproxen Sodium TABLET ORAL 20180801 20260630 ANDA ANDA090545 Medline Industries, LP NAPROXEN SODIUM 220 mg/1 100 TABLET in 1 BOTTLE (53329-688-30)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase