Application Information

This drug has been submitted to the FDA under the reference 076204/001.

Names and composition

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

Forms

ApplId/ProductId Drug name Active ingredient Form Strenght
076204/001 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 7.5MG
076204/002 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 15MG
077536/001 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 7.5MG
077536/002 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 15MG
078454/001 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 7.5MG
078454/002 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 15MG
090416/001 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 7.5MG
090416/002 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 15MG

Similar Active Ingredient

ApplId/ProductId Drug name Active ingredient Form Strenght
020312/001 UNIVASC MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
020312/002 UNIVASC MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
076204/001 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 7.5MG
076204/002 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 15MG
077536/001 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 7.5MG
077536/002 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 15MG
078454/001 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 7.5MG
078454/002 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 15MG
090416/001 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 7.5MG
090416/002 MOEXIPRIL HYDROCHLORIDE MOEXIPRIL HYDROCHLORIDE TABLET/ORAL 15MG

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