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=NDA019012"
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
29485-1465-4 29485-1465 HUMAN OTC DRUG Motrin IB Ibuprofen TABLET, FILM COATED ORAL 20000801 20251025 NDA NDA019012 Lil' Drug Store Products, Inc. IBUPROFEN 200 mg/1 2 POUCH in 1 PACKAGE (29485-1465-4) / 2 TABLET, FILM COATED in 1 POUCH
29485-6512-4 29485-6512 HUMAN OTC DRUG Motrin IB Ibuprofen TABLET, FILM COATED ORAL 20170825 20251231 NDA NDA019012 Lil' Drug Store Products, Inc. IBUPROFEN 200 mg/1 2 POUCH in 1 CARTON (29485-6512-4) / 2 TABLET, FILM COATED in 1 POUCH
29485-7006-3 29485-7006 HUMAN OTC DRUG Motrin IB Ibuprofen TABLET, FILM COATED ORAL 20170509 20251231 NDA NDA019012 Lil' Drug Store Products, Inc. IBUPROFEN 200 mg/1 30 POUCH in 1 BOX (29485-7006-3) / 2 TABLET, FILM COATED in 1 POUCH
29485-7938-6 29485-7938 HUMAN OTC DRUG Motrin IB Ibuprofen TABLET, FILM COATED ORAL 20170207 20260123 NDA NDA019012 Lil' Drug Store Products, Inc. IBUPROFEN 200 mg/1 3 POUCH in 1 PACKAGE (29485-7938-6) / 2 TABLET, FILM COATED in 1 POUCH
67751-120-01 67751-120 HUMAN OTC DRUG Motrin IB IBUPROFEN TABLET, FILM COATED ORAL 20160922 N/A NDA NDA019012 Navajo Manufacturing Company Inc. IBUPROFEN 200 mg/1 1 POUCH in 1 CARTON (67751-120-01) / 2 TABLET, FILM COATED in 1 POUCH
67751-120-02 67751-120 HUMAN OTC DRUG Motrin IB IBUPROFEN TABLET, FILM COATED ORAL 20160922 N/A NDA NDA019012 Navajo Manufacturing Company Inc. IBUPROFEN 200 mg/1 2 POUCH in 1 CARTON (67751-120-02) / 2 TABLET, FILM COATED in 1 POUCH
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