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DOLUTEGRAVIR, EMTRICITABINE and TENOFOVIR ALAFENAMIDE

AUROBINDO PHARMA USA · FDA-approved approved Quality 6/100

DOLUTEGRAVIR, EMTRICITABINE and TENOFOVIR ALAFENAMIDE is a drug developed by AUROBINDO PHARMA USA. It is currently FDA-approved.

At a glance

Generic nameDOLUTEGRAVIR, EMTRICITABINE and TENOFOVIR ALAFENAMIDE
SponsorAUROBINDO PHARMA USA
Therapeutic areaOther
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

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Frequently asked questions about DOLUTEGRAVIR, EMTRICITABINE and TENOFOVIR ALAFENAMIDE

What is DOLUTEGRAVIR, EMTRICITABINE and TENOFOVIR ALAFENAMIDE?

DOLUTEGRAVIR, EMTRICITABINE and TENOFOVIR ALAFENAMIDE is a pharmaceutical drug developed by AUROBINDO PHARMA USA.

Who makes DOLUTEGRAVIR, EMTRICITABINE and TENOFOVIR ALAFENAMIDE?

DOLUTEGRAVIR, EMTRICITABINE and TENOFOVIR ALAFENAMIDE is developed and marketed by AUROBINDO PHARMA USA (see full AUROBINDO PHARMA USA pipeline at /company/aurobindo-pharma-usa).

What development phase is DOLUTEGRAVIR, EMTRICITABINE and TENOFOVIR ALAFENAMIDE in?

DOLUTEGRAVIR, EMTRICITABINE and TENOFOVIR ALAFENAMIDE is FDA-approved (marketed).

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing