Application Information

This drug has been submitted to the FDA under the reference 074918/001.

Names and composition

"NALTREXONE HYDROCHLORIDE" is the commercial name of a drug composed of NALTREXONE HYDROCHLORIDE.

Forms

ApplId/ProductId Drug name Active ingredient Form Strenght
074918/001 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 50MG
075274/001 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 50MG
075434/001 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 50MG
076264/001 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 25MG
076264/002 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 50MG
076264/003 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 100MG
090356/001 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 50MG
091205/001 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 50MG
207905/001 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 50MG

Similar Active Ingredient

ApplId/ProductId Drug name Active ingredient Form Strenght
018932/001 REVIA NALTREXONE HYDROCHLORIDE TABLET/ORAL 50MG
074918/001 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 50MG
075274/001 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 50MG
075434/001 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 50MG
076264/001 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 25MG
076264/002 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 50MG
076264/003 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 100MG
090356/001 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 50MG
091205/001 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 50MG
207905/001 NALTREXONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE TABLET/ORAL 50MG

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