Application Information

This drug has been submitted to the FDA under the reference 206581/001.

Names and composition

"IBUPROFEN SODIUM" is the commercial name of a drug composed of IBUPROFEN SODIUM.

Forms

ApplId/ProductId Drug name Active ingredient Form Strenght
206581/001 IBUPROFEN SODIUM IBUPROFEN SODIUM TABLET/ORAL EQ 200MG BASE

Similar Active Ingredient

ApplId/ProductId Drug name Active ingredient Form Strenght
201803/001 ADVIL IBUPROFEN SODIUM TABLET/ORAL EQ 200MG BASE
206581/001 IBUPROFEN SODIUM IBUPROFEN SODIUM TABLET/ORAL EQ 200MG BASE

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