Application Information

This drug has been submitted to the FDA under the reference 079113/001.

Names and composition

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

Forms

ApplId/ProductId Drug name Active ingredient Form Strenght
079113/001 IBUPROFEN AND DIPHENHYDRAMINE CITRATE DIPHENHYDRAMINE CITRATE; IBUPROFEN TABLET/ORAL 38MG and 200MG
090619/001 IBUPROFEN AND DIPHENHYDRAMINE CITRATE DIPHENHYDRAMINE CITRATE; IBUPROFEN TABLET/ORAL 38MG and 200MG

Similar Active Ingredient

ApplId/ProductId Drug name Active ingredient Form Strenght
021394/001 ADVIL PM DIPHENHYDRAMINE CITRATE; IBUPROFEN TABLET/ORAL 38MG and 200MG
079113/001 IBUPROFEN AND DIPHENHYDRAMINE CITRATE DIPHENHYDRAMINE CITRATE; IBUPROFEN TABLET/ORAL 38MG and 200MG
090619/001 IBUPROFEN AND DIPHENHYDRAMINE CITRATE DIPHENHYDRAMINE CITRATE; IBUPROFEN TABLET/ORAL 38MG and 200MG

Ask a doctor

A licensed doctor will try to answer your question for free as quickly as possible. Free of charge during the beta period.

Related

Browse by letter
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

© Medications.li 2015-2017 - All rights reserved