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=ANDA077349"
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
50580-230-09 50580-230 HUMAN OTC DRUG Motrin IB Ibuprofen TABLET, FILM COATED ORAL 20170424 N/A ANDA ANDA077349 Kenvue Brands LLC IBUPROFEN 200 mg/1 50 POUCH in 1 CARTON (50580-230-09) / 2 TABLET, FILM COATED in 1 POUCH
67414-240-00 67414-240 HUMAN OTC DRUG Motrin IB IBUPROFEN TABLET, FILM COATED ORAL 20180125 N/A ANDA ANDA077349 Jones Healthcare Group - Packaging Services, Inc IBUPROFEN 200 mg/1 2500 POUCH in 1 BOX (67414-240-00) / 2 TABLET, FILM COATED in 1 POUCH
67414-240-09 67414-240 HUMAN OTC DRUG Motrin IB IBUPROFEN TABLET, FILM COATED ORAL 20180125 N/A ANDA ANDA077349 Jones Healthcare Group - Packaging Services, Inc IBUPROFEN 200 mg/1 50 POUCH in 1 CARTON (67414-240-09) / 2 TABLET, FILM COATED in 1 POUCH
69168-390-30 69168-390 HUMAN OTC DRUG Ibuprofen 200mg Ibuprofen 200mg TABLET, FILM COATED ORAL 20141223 N/A ANDA ANDA077349 Allegiant Health IBUPROFEN 200 mg/1 1 BOTTLE in 1 CARTON (69168-390-30) / 30 TABLET, FILM COATED in 1 BOTTLE
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