Application Information

This drug has been submitted to the FDA under the reference 078316/001.

Names and composition

"OXYCODONE HYDROCHLORIDE AND IBUPROFEN" is the commercial name of a drug composed of IBUPROFEN and OXYCODONE HYDROCHLORIDE.

Forms

ApplId/ProductId Drug name Active ingredient Form Strenght
078316/001 OXYCODONE HYDROCHLORIDE AND IBUPROFEN IBUPROFEN; OXYCODONE HYDROCHLORIDE TABLET/ORAL 400MG and 5MG
078394/001 OXYCODONE HYDROCHLORIDE AND IBUPROFEN IBUPROFEN; OXYCODONE HYDROCHLORIDE TABLET/ORAL 400MG and 5MG
078769/001 OXYCODONE HYDROCHLORIDE AND IBUPROFEN IBUPROFEN; OXYCODONE HYDROCHLORIDE TABLET/ORAL 400MG and 5MG

Similar Active Ingredient

ApplId/ProductId Drug name Active ingredient Form Strenght
021378/001 COMBUNOX IBUPROFEN; OXYCODONE HYDROCHLORIDE TABLET/ORAL 400MG and 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
078316/001 OXYCODONE HYDROCHLORIDE AND IBUPROFEN IBUPROFEN; OXYCODONE HYDROCHLORIDE TABLET/ORAL 400MG and 5MG
078394/001 OXYCODONE HYDROCHLORIDE AND IBUPROFEN IBUPROFEN; OXYCODONE HYDROCHLORIDE TABLET/ORAL 400MG and 5MG
078769/001 OXYCODONE HYDROCHLORIDE AND IBUPROFEN IBUPROFEN; OXYCODONE HYDROCHLORIDE TABLET/ORAL 400MG and 5MG

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