Application Information

This drug has been submitted to the FDA under the reference 090397/001.

Names and composition

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

Forms

ApplId/ProductId Drug name Active ingredient Form Strenght
090397/001 IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN CAPSULE/ORAL 25MG and EQ 200MG FREE ACID AND POTASSIUM SALT
200888/001 IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN CAPSULE/ORAL 25MG and EQ 200MG FREE ACID AND POTASSIUM SALT

Similar Active Ingredient

ApplId/ProductId Drug name Active ingredient Form Strenght
021393/001 ADVIL PM DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN CAPSULE/ORAL 25MG and EQ 200MG FREE ACID AND POTASSIUM SALT
090397/001 IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN CAPSULE/ORAL 25MG and EQ 200MG FREE ACID AND POTASSIUM SALT
200888/001 IBUPROFEN AND DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN CAPSULE/ORAL 25MG and EQ 200MG FREE ACID AND POTASSIUM SALT

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