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
37808-652-71 37808-652 HUMAN OTC DRUG naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20171114 N/A ANDA ANDA074661 H E B NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (37808-652-71) / 50 TABLET, FILM COATED in 1 BOTTLE
37808-652-62 37808-652 HUMAN OTC DRUG naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20171114 N/A ANDA ANDA074661 H E B NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (37808-652-62) / 24 TABLET, FILM COATED in 1 BOTTLE
37808-631-82 37808-631 HUMAN OTC DRUG naproxen sodium Naproxen sodium TABLET, FILM COATED ORAL 20171114 N/A ANDA ANDA074661 H E B NAPROXEN SODIUM 220 mg/1 200 TABLET, FILM COATED in 1 BOTTLE (37808-631-82)
37808-713-79 37808-713 HUMAN OTC DRUG naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20171003 N/A ANDA ANDA074661 H E B NAPROXEN SODIUM 220 mg/1 400 TABLET, FILM COATED in 1 BOTTLE (37808-713-79)
69842-811-78 69842-811 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20180626 N/A ANDA ANDA074661 CVS Pharmacy NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (69842-811-78) / 100 TABLET, FILM COATED in 1 BOTTLE
69842-811-90 69842-811 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20180509 N/A ANDA ANDA074661 CVS Pharmacy NAPROXEN SODIUM 220 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (69842-811-90)
69842-811-62 69842-811 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20180509 N/A ANDA ANDA074661 CVS Pharmacy NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (69842-811-62) / 24 TABLET, FILM COATED in 1 BOTTLE
69842-811-71 69842-811 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20180509 N/A ANDA ANDA074661 CVS Pharmacy NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (69842-811-71) / 50 TABLET, FILM COATED in 1 BOTTLE
69842-811-75 69842-811 HUMAN OTC DRUG Naproxen Sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220408 N/A ANDA ANDA074661 CVS Pharmacy NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (69842-811-75) / 90 TABLET, FILM COATED in 1 BOTTLE
11673-909-75 11673-909 HUMAN OTC DRUG up and up naproxen sodium naproxen sodium TABLET, FILM COATED ORAL 20220210 N/A ANDA ANDA074661 Target Corporation NAPROXEN SODIUM 220 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (11673-909-75)
11822-0140-1 11822-0140 HUMAN OTC DRUG Naproxen Sodium Naproxen sodium TABLET, FILM COATED ORAL 20160701 N/A ANDA ANDA074661 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 270 TABLET, FILM COATED in 1 BOTTLE (11822-0140-1)
11822-0490-5 11822-0490 HUMAN OTC DRUG naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20211229 N/A ANDA ANDA074661 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (11822-0490-5) / 90 TABLET, FILM COATED in 1 BOTTLE
11822-0490-7 11822-0490 HUMAN OTC DRUG naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20010516 N/A ANDA ANDA074661 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (11822-0490-7) / 100 TABLET, FILM COATED in 1 BOTTLE
11822-0507-9 11822-0507 HUMAN OTC DRUG naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20220117 N/A ANDA ANDA074661 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (11822-0507-9) / 90 TABLET, FILM COATED in 1 BOTTLE
11822-0507-1 11822-0507 HUMAN OTC DRUG naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20010625 N/A ANDA ANDA074661 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (11822-0507-1) / 50 TABLET, FILM COATED in 1 BOTTLE
11822-0507-3 11822-0507 HUMAN OTC DRUG naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20140528 N/A ANDA ANDA074661 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (11822-0507-3) / 24 TABLET, FILM COATED in 1 BOTTLE
11822-0507-7 11822-0507 HUMAN OTC DRUG naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20010516 N/A ANDA ANDA074661 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (11822-0507-7) / 100 TABLET, FILM COATED in 1 BOTTLE
11822-0507-8 11822-0507 HUMAN OTC DRUG naproxen sodium Naproxen Sodium TABLET, FILM COATED ORAL 20010531 N/A ANDA ANDA074661 Rite Aid Corporation NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (11822-0507-8) / 200 TABLET, FILM COATED in 1 BOTTLE
36800-140-82 36800-140 HUMAN OTC DRUG Topcare All Day Pain Relief Naproxen sodium TABLET, FILM COATED ORAL 20071203 N/A ANDA ANDA074661 Topco Associates LLC NAPROXEN SODIUM 220 mg/1 200 TABLET, FILM COATED in 1 BOTTLE (36800-140-82)
55910-481-62 55910-481 HUMAN OTC DRUG DG Health Naproxen Sodium naproxen sodium TABLET, FILM COATED ORAL 20210526 N/A ANDA ANDA074661 Dolgencorp, LLC NAPROXEN SODIUM 220 mg/1 1 BOTTLE in 1 CARTON (55910-481-62) / 24 TABLET, FILM COATED in 1 BOTTLE
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