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EMA Product

Somac Control

Product approved by European Medicines Agency (EU)

Basic Information

Somac Control

Regulatory Information

EMEA/H/C/001098

Authorised

June 12, 2009

February 19, 2009

16

May 24, 2023

Company Information

Germany

Byk-Gulden-Strasse 2 D-78467 Konstanz

Takeda GmbH

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Short-term treatment of reflux symptoms (e.g. heartburn, acid regurgitation) in adults.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Somac Control. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Somac Control.

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