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EMA Product

Lamivudine Teva Pharma B.V.

Product approved by European Medicines Agency (EU)

Basic Information

Lamivudine Teva Pharma B.V.

Regulatory Information

EMEA/H/C/001111

Authorised

December 10, 2009

19

April 21, 2023

Company Information

the netherlands

Teva B.V. Swensweg 5 2031 GA Haarlem

Teva Pharma B.V.

Drug Classification

Generic Medicine

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Lamivudine Teva Pharma B.V. is indicated as part of antiretroviral combination therapy for the treatment of human-immunodeficiency-virus (HIV)-infected adults and children.

Overview Summary

This is a summary of the European public assessment report (EPAR). It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the studies performed, to reach its recommendations on how to use the medicine. If you need more information about your medical condition or your treatment, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist. If you want more information on the basis for the CHMP recommendations, read the scientific discussion (also part of the EPAR).

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