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EMA Product

Telmisartan Teva Pharma

Product approved by European Medicines Agency (EU)

Basic Information

Telmisartan Teva Pharma

Regulatory Information

EMEA/H/C/002511

Authorised

October 3, 2011

July 21, 2011

10

October 26, 2021

Company Information

the netherlands

Swensweg 5 2031GA Haarlem

Teva Pharma B.V.

Drug Classification

Generic Medicine

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Treatment of essential hypertension in adults.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Telmisartan Teva Pharma. 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 Telmisartan Teva Pharma.

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