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Dovato (dolutegravir and lamivudine) information for Healthcare Professionals registered in Ireland View Dovato EMA approval details, including marketing authorisation, regulatory status, and therapeutic informationDOVATO Film-coated tablet Ref [10718] Active ingredients: Dolutegravir Lamivudine Lamivudine and Dolutegravir Source: European Medicines Agency (EU) Revision Year: 2023 Publisher: ViiV Healthcare BV, Van Asch van Wijckstraat 55H, 3811 LP Amersfoort, NetherlandsUse DrugPatentWatch com’s Dovato page to view the European patent and exclusivity landscape, including the patent identifiers and timelines used to estimate when generics might be able to launch Discover DOVATO (dolutegravir lamivudine), a complete HIV-1 treatment for people 12 years and older who weigh at least 55 lbs See full Safety and Prescribing Information, including Boxed Warning This page intends to provide information presented at recent congresses relevant to your unsolicited enquiry Regulations vary by country, and some information may be off label (not authorised) in your country Please refer to local product information before prescribing ViiV Healthcare do not advocate off -label use of their medicines DOVATO is indicated for the treatment of Human Immunodeficiency Virus type 1 (HIV-1) infection in adults and adolescents above 12 years of age weighing at least 40 kg, with no known or suspected resistance to the integrase inhibitor class, or lamivudine