Application Information

This drug has been submitted to the FDA under the reference 208369/001.

Names and composition

"GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE" is the commercial name of a drug composed of GUAIFENESIN and PSEUDOEPHEDRINE HYDROCHLORIDE.

Forms

ApplId/ProductId Drug name Active ingredient Form Strenght
208369/001 GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE GUAIFENESIN;PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE/ORAL 600MG and 60MG
208369/002 GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE GUAIFENESIN;PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE/ORAL 1200MG and 120MG

Similar Active Ingredient

ApplId/ProductId Drug name Active ingredient Form Strenght
208369/001 GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE GUAIFENESIN;PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE/ORAL 600MG and 60MG
208369/002 GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE GUAIFENESIN;PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE/ORAL 1200MG and 120MG

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