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=ANDA074661"
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
55910-729-62 55910-729 HUMAN OTC DRUG dg health naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20190612 N/A ANDA ANDA074661 Dolgencorp, LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (55910-729-62) / 24 TABLET, FILM COATED in 1 BOTTLE
55910-729-71 55910-729 HUMAN OTC DRUG dg health naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20190612 N/A ANDA ANDA074661 Dolgencorp, LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (55910-729-71) / 50 TABLET, FILM COATED in 1 BOTTLE
55910-729-78 55910-729 HUMAN OTC DRUG dg health naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20200324 N/A ANDA ANDA074661 Dolgencorp, LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (55910-729-78) / 100 TABLET, FILM COATED in 1 BOTTLE
36800-696-75 36800-696 HUMAN OTC DRUG topcare back and muscle pain naproxen sodium TABLET, FILM COATED ORAL 20211213 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-696-75) / 90 TABLET, FILM COATED in 1 BOTTLE
36800-696-78 36800-696 HUMAN OTC DRUG topcare back and muscle pain naproxen sodium TABLET, FILM COATED ORAL 20190625 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (36800-696-78) / 100 TABLET, FILM COATED in 1 BOTTLE
21130-802-82 21130-802 HUMAN OTC DRUG signature care naproxen sodium Naproxen sodium TABLET, FILM COATED ORAL 20180702 N/A ANDA ANDA074661 Safeway NAPROXEN SODIUM 220 mg/1 200 TABLET, FILM COATED in 1 BOTTLE (21130-802-82)
0113-0901-62 0113-0901 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20140423 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0113-0901-62) / 24 TABLET, FILM COATED in 1 BOTTLE
0113-0901-71 0113-0901 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20140423 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0113-0901-71) / 50 TABLET, FILM COATED in 1 BOTTLE
0113-0901-75 0113-0901 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20211208 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0113-0901-75) / 90 TABLET, FILM COATED in 1 BOTTLE
0113-1412-71 0113-1412 HUMAN OTC DRUG good sense naproxen sodium naproxen sodium TABLET, FILM COATED ORAL 20211109 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0113-1412-71) / 50 TABLET, FILM COATED in 1 BOTTLE
0113-4368-62 0113-4368 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20140331 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0113-4368-62) / 24 TABLET, FILM COATED in 1 BOTTLE
0113-4368-71 0113-4368 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20140331 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0113-4368-71) / 50 TABLET, FILM COATED in 1 BOTTLE
0113-4368-75 0113-4368 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20211208 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0113-4368-75) / 90 TABLET, FILM COATED in 1 BOTTLE
0113-4368-78 0113-4368 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20140331 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0113-4368-78) / 100 TABLET, FILM COATED in 1 BOTTLE
0113-4368-79 0113-4368 HUMAN OTC DRUG Good Sense Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20180619 N/A ANDA ANDA074661 L. Perrigo Company NAPROXEN SODIUM 220 mg/1 400 TABLET, FILM COATED in 1 BOTTLE (0113-4368-79)
0363-0140-75 0363-0140 HUMAN OTC DRUG pain relief Naproxen sodium TABLET, FILM COATED ORAL 20220413 N/A ANDA ANDA074661 Walgreen Company NAPROXEN SODIUM 220 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (0363-0140-75)
0363-0368-62 0363-0368 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 19970114 20250430 ANDA ANDA074661 Walgreen Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0363-0368-62) / 24 TABLET, FILM COATED in 1 BOTTLE
0363-0368-71 0363-0368 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 19970114 N/A ANDA ANDA074661 Walgreen Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0363-0368-71) / 50 TABLET, FILM COATED in 1 BOTTLE
0363-0368-75 0363-0368 HUMAN OTC DRUG All Day Pain Relief Naproxen Sodium TABLET, FILM COATED ORAL 20220726 N/A ANDA ANDA074661 Walgreen Company NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (0363-0368-75) / 90 TABLET, FILM COATED in 1 BOTTLE
0363-0938-82 0363-0938 HUMAN OTC DRUG all day pain relief Naproxen Sodium TABLET, FILM COATED ORAL 20140731 N/A ANDA ANDA074661 Walgreen Company NAPROXEN SODIUM 200 mg/1 200 TABLET, FILM COATED in 1 BOTTLE (0363-0938-82)
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