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=NDA201803"
符合检索条件的记录共 16 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
0573-0133-01 0573-0133 HUMAN OTC DRUG Advil ibuprofen sodium TABLET, COATED ORAL 20140811 N/A NDA NDA201803 Haleon US Holdings LLC IBUPROFEN SODIUM 256 mg/1 3000 PACKET in 1 CASE (0573-0133-01) / 2 TABLET, COATED in 1 PACKET
0573-0133-02 0573-0133 HUMAN OTC DRUG Advil ibuprofen sodium TABLET, COATED ORAL 20130708 N/A NDA NDA201803 Haleon US Holdings LLC IBUPROFEN SODIUM 256 mg/1 50 PACKET in 1 TRAY (0573-0133-02) / 2 TABLET, COATED in 1 PACKET
0573-0133-04 0573-0133 HUMAN OTC DRUG Advil ibuprofen sodium TABLET, COATED ORAL 20130708 N/A NDA NDA201803 Haleon US Holdings LLC IBUPROFEN SODIUM 256 mg/1 2 PACKET in 1 BLISTER PACK (0573-0133-04) / 2 TABLET, COATED in 1 PACKET
0573-0133-05 0573-0133 HUMAN OTC DRUG Advil ibuprofen sodium TABLET, COATED ORAL 20130708 N/A NDA NDA201803 Haleon US Holdings LLC IBUPROFEN SODIUM 256 mg/1 2 PACKET in 1 CARTON (0573-0133-05) / 2 TABLET, COATED in 1 PACKET
0573-0133-20 0573-0133 HUMAN OTC DRUG Advil ibuprofen sodium TABLET, COATED ORAL 20130708 N/A NDA NDA201803 Haleon US Holdings LLC IBUPROFEN SODIUM 256 mg/1 1 BOTTLE in 1 CARTON (0573-0133-20) / 20 TABLET, COATED in 1 BOTTLE
0573-0133-40 0573-0133 HUMAN OTC DRUG Advil ibuprofen sodium TABLET, COATED ORAL 20130708 N/A NDA NDA201803 Haleon US Holdings LLC IBUPROFEN SODIUM 256 mg/1 1 BOTTLE in 1 CARTON (0573-0133-40) / 40 TABLET, COATED in 1 BOTTLE
0573-0133-41 0573-0133 HUMAN OTC DRUG Advil ibuprofen sodium TABLET, COATED ORAL 20150812 N/A NDA NDA201803 Haleon US Holdings LLC IBUPROFEN SODIUM 256 mg/1 1 BOTTLE in 1 CARTON (0573-0133-41) / 40 TABLET, COATED in 1 BOTTLE
0573-0133-80 0573-0133 HUMAN OTC DRUG Advil ibuprofen sodium TABLET, COATED ORAL 20130708 N/A NDA NDA201803 Haleon US Holdings LLC IBUPROFEN SODIUM 256 mg/1 1 BOTTLE in 1 CARTON (0573-0133-80) / 80 TABLET, COATED in 1 BOTTLE
0573-0133-81 0573-0133 HUMAN OTC DRUG Advil ibuprofen sodium TABLET, COATED ORAL 20130708 N/A NDA NDA201803 Haleon US Holdings LLC IBUPROFEN SODIUM 256 mg/1 1 BOTTLE in 1 CARTON (0573-0133-81) / 100 TABLET, COATED in 1 BOTTLE
0573-0133-88 0573-0133 HUMAN OTC DRUG Advil ibuprofen sodium TABLET, COATED ORAL 20130708 N/A NDA NDA201803 Haleon US Holdings LLC IBUPROFEN SODIUM 256 mg/1 2 BOTTLE in 1 PACKAGE (0573-0133-88) / 120 TABLET, COATED in 1 BOTTLE
0573-0133-89 0573-0133 HUMAN OTC DRUG Advil ibuprofen sodium TABLET, COATED ORAL 20130708 N/A NDA NDA201803 Haleon US Holdings LLC IBUPROFEN SODIUM 256 mg/1 1 BOTTLE in 1 CARTON (0573-0133-89) / 160 TABLET, COATED in 1 BOTTLE
0573-0133-91 0573-0133 HUMAN OTC DRUG Advil ibuprofen sodium TABLET, COATED ORAL 20141201 N/A NDA NDA201803 Haleon US Holdings LLC IBUPROFEN SODIUM 256 mg/1 1 BOTTLE in 1 CARTON (0573-0133-91) / 180 TABLET, COATED in 1 BOTTLE
0573-0134-20 0573-0134 HUMAN OTC DRUG Advil ibuprofen sodium TABLET, COATED ORAL 20130708 N/A NDA NDA201803 Haleon US Holdings LLC IBUPROFEN SODIUM 256 mg/1 1 BOTTLE in 1 CARTON (0573-0134-20) / 20 TABLET, COATED in 1 BOTTLE
0573-0134-80 0573-0134 HUMAN OTC DRUG Advil ibuprofen sodium TABLET, COATED ORAL 20130708 N/A NDA NDA201803 Haleon US Holdings LLC IBUPROFEN SODIUM 256 mg/1 1 BOTTLE in 1 CARTON (0573-0134-80) / 80 TABLET, COATED in 1 BOTTLE
0573-0230-20 0573-0230 HUMAN OTC DRUG Advil Menstrual Pain ibuprofen sodium TABLET, COATED ORAL 20160701 N/A NDA NDA201803 Haleon US Holdings LLC IBUPROFEN SODIUM 256 mg/1 1 BOTTLE in 1 CARTON (0573-0230-20) / 20 TABLET, COATED in 1 BOTTLE
0573-0230-40 0573-0230 HUMAN OTC DRUG Advil Menstrual Pain ibuprofen sodium TABLET, COATED ORAL 20160701 N/A NDA NDA201803 Haleon US Holdings LLC IBUPROFEN SODIUM 256 mg/1 1 BOTTLE in 1 CARTON (0573-0230-40) / 40 TABLET, COATED in 1 BOTTLE
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