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Application Number Application Type Drug Name Active Ingredients Dosage Form/Route Approval Date Company
218684 ANDA IBUPROFEN AND FAMOTIDINE FAMOTIDINE; IBUPROFEN TABLET;ORAL ZYDUS PHARMS
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
217241 ANDA ACETAMINOPHEN AND IBUPROFEN ACETAMINOPHEN; IBUPROFEN TABLET;ORAL STRIDES PHARMA
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 IBUPROFEN AND FAMOTIDINE 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
214789 ANDA IBUPROFEN IBUPROFEN SUSPENSION;ORAL PAI HOLDINGS PHARM
214699 ANDA IBUPROFEN IBUPROFEN TABLET;ORAL 2021-09-13 ALKEM LABS LTD