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=ANDA207095"
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
58624-7007-0 58624-7007 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220405 N/A ANDA ANDA207095 Shandong Xinhua Pharmaceutical Co., Ltd. IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (58624-7007-0) / 24 TABLET, FILM COATED in 1 BOTTLE
58624-7011-0 58624-7011 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220405 N/A ANDA ANDA207095 Shandong Xinhua Pharmaceutical Co., Ltd. IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (58624-7011-0) / 24 TABLET, FILM COATED in 1 BOTTLE
69168-467-03 69168-467 HUMAN OTC DRUG Ibuprofen 200mg Ibuprofen 200mg TABLET ORAL 20241017 N/A ANDA ANDA207095 Allegiant Health IBUPROFEN 200 mg/1 250 TABLET in 1 BOTTLE (69168-467-03)
69168-467-05 69168-467 HUMAN OTC DRUG Ibuprofen 200mg Ibuprofen 200mg TABLET ORAL 20241017 N/A ANDA ANDA207095 Allegiant Health IBUPROFEN 200 mg/1 500 TABLET in 1 BOTTLE (69168-467-05)
69168-467-32 69168-467 HUMAN OTC DRUG Ibuprofen 200mg Ibuprofen 200mg TABLET ORAL 20241017 N/A ANDA ANDA207095 Allegiant Health IBUPROFEN 200 mg/1 100 TABLET in 1 BOTTLE (69168-467-32)
58624-7008-0 58624-7008 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220405 N/A ANDA ANDA207095 Shandong Xinhua Pharmaceutical Co., Ltd. IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (58624-7008-0) / 24 TABLET, FILM COATED in 1 BOTTLE
58624-7012-0 58624-7012 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220405 N/A ANDA ANDA207095 Shandong Xinhua Pharmaceutical Co., Ltd. IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (58624-7012-0) / 24 TABLET, FILM COATED in 1 BOTTLE
83059-0049-3 83059-0049 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, COATED ORAL 20241008 N/A ANDA ANDA207095 Shield Pharmaceuticals Corp IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (83059-0049-3) / 30 TABLET, COATED in 1 BOTTLE
58624-7009-0 58624-7009 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220405 N/A ANDA ANDA207095 Shandong Xinhua Pharmaceutical Co., Ltd. IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (58624-7009-0) / 24 TABLET, FILM COATED in 1 BOTTLE
83059-0019-3 83059-0019 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, COATED ORAL 20240125 N/A ANDA ANDA207095 Shield Pharmaceuticals Corp IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (83059-0019-3) / 30 TABLET, COATED in 1 BOTTLE
69396-141-01 69396-141 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20230808 N/A ANDA ANDA207095 Trifecta Pharmaceuticals USA LLC IBUPROFEN 200 mg/1 50 PACKET in 1 BOX (69396-141-01) / 2 TABLET in 1 PACKET
69396-141-05 69396-141 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20230808 N/A ANDA ANDA207095 Trifecta Pharmaceuticals USA LLC IBUPROFEN 200 mg/1 10000 PACKET in 1 BAG (69396-141-05) / 2 TABLET in 1 PACKET
58624-7010-0 58624-7010 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20220405 N/A ANDA ANDA207095 Shandong Xinhua Pharmaceutical Co., Ltd. IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (58624-7010-0) / 24 TABLET, FILM COATED in 1 BOTTLE
83059-0020-4 83059-0020 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET, COATED ORAL 20240126 N/A ANDA ANDA207095 Shield Pharmaceuticals Corp IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (83059-0020-4) / 40 TABLET, COATED in 1 BOTTLE
69396-145-01 69396-145 HUMAN OTC DRUG Ibuprofen Ibuprofen TABLET ORAL 20230808 N/A ANDA ANDA207095 Trifecta Pharmaceuticals USA LLC IBUPROFEN 200 mg/1 50 PACKET in 1 BOX (69396-145-01) / 2 TABLET in 1 PACKET
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase