• English
  • 简体中文
Login Register
Current Location: Home > FDA Approved Drug Products Feedback Help
-
-
Application Number Application Type Drug Name Active Ingredients Dosage Form/Route Approval Date Company
218359 ANDA ACETAMINOPHEN AND IBUPROFEN ACETAMINOPHEN; IBUPROFEN TABLET;ORAL AUROBINDO PHARMA LTD
218311 ANDA ACETAMINOPHEN AND IBUPROFEN ACETAMINOPHEN; IBUPROFEN TABLET;ORAL GLENMARK PHARMS LTD
218247 ANDA ACETAMINOPHEN AND IBUPROFEN ACETAMINOPHEN; IBUPROFEN TABLET;ORAL DR REDDYS
217261 ANDA IBUPROFEN IBUPROFEN SUSPENSION/DROPS;ORAL TARO
217236 ANDA IBUPROFEN IBUPROFEN CAPSULE;ORAL PATHEON SOFTGELS
216999 ANDA ACETAMINOPHEN AND IBUPROFEN ACETAMINOPHEN; IBUPROFEN TABLET;ORAL BIONPHARMA
216994 ANDA ACETAMINOPHEN AND IBUPROFEN ACETAMINOPHEN; IBUPROFEN TABLET;ORAL MARKSANS PHARMA
216814 ANDA IBUPROFEN AND FAMOTIDINE FAMOTIDINE; IBUPROFEN TABLET;ORAL 2023-03-15 ASCENT PHARMS INC
216592 ANDA ACETAMINOPHEN AND IBUPROFEN ACETAMINOPHEN; IBUPROFEN TABLET;ORAL GRANULES
216204 ANDA IBUPROFEN AND DIPHENHYDRAMINE CITRATE DIPHENHYDRAMINE CITRATE; IBUPROFEN TABLET;ORAL 2022-05-31 AUROBINDO PHARMA
215925 ANDA FAMOTIDINE AND IBUPROFEN FAMOTIDINE; IBUPROFEN TABLET;ORAL TORRENT
215777 ANDA IBUPROFEN IBUPROFEN CAPSULE;ORAL AUROBINDO PHARMA LTD
215320 NDA COMBOGESIC IV ACETAMINOPHEN; IBUPROFEN SODIUM SOLUTION;INTRAVENOUS HIKMA
215318 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 2022-03-30 YICHANG HUMANWELL
215311 ANDA IBUPROFEN IBUPROFEN SUSPENSION;ORAL 2022-05-27 STRIDES PHARMA
214836 ANDA ACETAMINOPHEN AND IBUPROFEN ACETAMINOPHEN; IBUPROFEN TABLET;ORAL 2023-02-28 L PERRIGO CO
214699 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 2021-09-13 ALKEM LABS LTD
214071 ANDA IBUPROFEN IBUPROFEN SUSPENSION/DROPS;ORAL 2022-06-09 STRIDES PHARMA
214003 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 2020-10-19 YICHANG HUMANWELL
213794 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 2020-05-08 AUROBINDO PHARMA LTD