Application Information

This drug has been submitted to the FDA under the reference 075842/001.

Names and composition

"OXAPROZIN" is the commercial name of a drug composed of OXAPROZIN.

Forms

ApplId/ProductId Drug name Active ingredient Form Strenght
075842/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075843/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075844/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075845/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075846/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075847/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075848/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075849/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075850/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075851/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075855/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075987/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
208633/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG

Similar Active Ingredient

ApplId/ProductId Drug name Active ingredient Form Strenght
018841/004 DAYPRO OXAPROZIN TABLET/ORAL 600MG
075842/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075843/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075844/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075845/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075846/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075847/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075848/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075849/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075850/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075851/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075855/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
075987/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG
208633/001 OXAPROZIN OXAPROZIN TABLET/ORAL 600MG

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