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          1. 列表页商品名字段中有红色标记P代表该数据有专利信息;当使用各个专利到期时间检索条件时,“有无专利”默认为有。


          2. 批准日期显示1982-01-01的,实际为1982-01-01之前。


          3. 更多参比制剂一次性进口信息

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          申请号 产品号 商品名 活性成分 活性成分 剂型/给药途径 规格/剂量 申请机构 批准时间 参比制剂 标准制剂 市场状态 TE
          (NDA) 215320 001 COMBOGESIC IVP ACETAMINOPHEN; IBUPROFEN SODIUM 布洛芬钠;对乙酰氨基酚 SOLUTION;INTRAVENOUS 1GM/100ML (10MG/ML);EQ 300MG BASE/100ML (EQ 3MG BASE/ML) HIKMA 2023-10-17 Yes Yes RX
          (NDA) 211733 001 ADVIL DUAL ACTION WITH ACETAMINOPHENP ACETAMINOPHEN; IBUPROFEN 对乙酰氨基酚;布洛芬 TABLET;ORAL 250MG;125MG HALEON US HOLDINGS 2020-02-28 Yes Yes OTC
          (NDA) 209471 001 COMBOGESICP ACETAMINOPHEN; IBUPROFEN 对乙酰氨基酚;布洛芬 TABLET;ORAL 325MG;97.5MG AFT PHARMS US 2023-03-01 Yes Yes RX
          (NDA) 201803 001 ADVIL IBUPROFEN SODIUM 布洛芬钠 TABLET;ORAL EQ 200MG BASE HALEON US HOLDINGS 2012-06-12 Yes Yes OTC
          (NDA) 022565 001 ADVIL CONGESTION RELIEF IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE 布洛芬;盐酸去氧肾上腺素 TABLET;ORAL 200MG;10MG HALEON US HOLDINGS 2010-05-27 Yes Yes OTC
          (NDA) 022519 001 DUEXISP FAMOTIDINE; IBUPROFEN 法莫替丁;布洛芬 TABLET;ORAL 26.6MG;800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** HORIZON 2011-04-23 Yes No DISCN
          (NDA) 022348 002 CALDOLORP IBUPROFEN 布洛芬 SOLUTION;INTRAVENOUS 800MG/8ML (100MG/ML) CUMBERLAND PHARMS 2009-06-11 Yes Yes RX
          (NDA) 022348 003 CALDOLORP IBUPROFEN 布洛芬 SOLUTION;INTRAVENOUS 800MG/200ML (4MG/ML) CUMBERLAND PHARMS 2019-01-25 Yes Yes RX
          (NDA) 022113 001 ADVIL ALLERGY AND CONGESTION RELIEF CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE 马来酸氯苯那敏;布洛芬;盐酸去氧肾上腺素 TABLET;ORAL 4MG;200MG;10MG HALEON US HOLDINGS 2011-12-21 Yes Yes OTC
          (NDA) 022113 002 ADVIL MULTI-SYMPTOM COLD & FLU CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE 马来酸氯苯那敏;布洛芬;盐酸去氧肾上腺素 TABLET;ORAL 4MG;200MG;10MG HALEON US HOLDINGS 2017-04-28 Yes Yes OTC
          (NDA) 021903 001 NEOPROFENP IBUPROFEN LYSINE INJECTABLE;INTRAVENOUS EQ 20MG BASE/2ML (EQ 10MG BASE/ML) RECORDATI RARE 2006-04-13 Yes Yes RX AP
          (NDA) 021587 001 CHILDREN'S ADVIL ALLERGY SINUS CHLORPHENIRAMINE MALEATE; IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE 马来酸氯苯那敏;布洛芬;盐酸伪麻黄碱 SUSPENSION;ORAL 1MG/5ML;100MG/5ML;15MG/5ML HALEON US HOLDINGS 2004-02-24 Yes Yes OTC
          (NDA) 021472 001 MIDOL LIQUID GELS IBUPROFEN 布洛芬 CAPSULE;ORAL 200MG BIONPHARMA 2002-10-18 Yes Yes OTC
          (NDA) 021441 001 ADVIL ALLERGY SINUSP CHLORPHENIRAMINE MALEATE; IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE 马来酸氯苯那敏;布洛芬;盐酸伪麻黄碱 TABLET;ORAL 2MG;200MG;30MG HALEON US HOLDINGS 2002-12-19 Yes Yes OTC
          (NDA) 021394 001 ADVIL PM DIPHENHYDRAMINE CITRATE; IBUPROFEN 枸橼酸苯海拉明;布洛芬 TABLET;ORAL 38MG;200MG HALEON US HOLDINGS 2005-12-21 Yes Yes OTC
          (NDA) 021393 001 ADVIL PM DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN 盐酸苯海拉明;布洛芬 CAPSULE;ORAL 25MG;EQ 200MG FREE ACID AND POTASSIUM SALT HALEON US HOLDINGS 2005-12-21 Yes Yes OTC
          (NDA) 021378 001 COMBUNOX IBUPROFEN; OXYCODONE HYDROCHLORIDE 布洛芬;盐酸羟考酮 TABLET;ORAL 400MG;5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** FOREST LABS 2004-11-26 Yes No DISCN
          (NDA) 021374 001 ADVIL COLD AND SINUS IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE 布洛芬;盐酸伪麻黄碱 CAPSULE;ORAL EQ 200MG FREE ACID AND POTASSIUM SALT;30MG HALEON US HOLDINGS 2002-05-30 Yes Yes OTC
          (NDA) 021128 001 CHILDREN'S MOTRIN COLD IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE 布洛芬;盐酸伪麻黄碱 SUSPENSION;ORAL 100MG/5ML;15MG/5ML KENVUE BRANDS 2000-08-01 Yes Yes OTC
          (NDA) 020812 001 PEDIATRIC ADVIL IBUPROFEN 布洛芬 SUSPENSION/DROPS;ORAL 100MG/2.5ML HALEON US HOLDINGS 1998-01-30 Yes No DISCN
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