Abacavir, Dolutegravir, and Lamivudine
Abacavir, dolutegravir, and lamivudine is a three-drug combination used to treat HIV-1 infection in adults and in children aged at least 3 months who weigh at least 6 kg.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 1 clinical label set within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
Triumeq (abacavir, dolutegravir, and lamivudine) is a well-established, once-daily, single-tablet HIV-1 treatment, on the market since about 2014 and available only as the brand, that pairs dolutegravir, which blocks integrase, with abacavir and lamivudine, which block reverse transcriptase (two enzymes the virus needs to multiply). Most people tolerate it well, usually noticing only trouble sleeping, headache or tiredness. Its main boxed warning is a serious, sometimes fatal allergic reaction to abacavir (fever, rash, stomach upset, cough or feeling very unwell), so stop it, get help and never restart it. A second boxed warning covers hepatitis B flares if you stop it, so expect tests for hepatitis B and the HLA-B*5701 gene first.
Clinical pearls
- Never combine it with dofetilide, a heart rhythm medicine, because dolutegravir can push dofetilide to dangerous levels.
- If you take metformin or dalfampridine, tell that prescriber, since dolutegravir can raise levels of both.
- Triumeq tablets and Triumeq PD tablets for oral suspension contain different dolutegravir amounts, so never swap one for the other.
- The abacavir reaction usually starts within the first six weeks, so be most alert early, though it can happen anytime.
⚠️ FDA Boxed Warning — the FDA’s strongest safety alert ▾
Serious, sometimes fatal allergic reactions can happen with the abacavir in this medicine. They can affect several parts of the body at once. Your risk is higher if you carry the HLA-B*5701 gene, so you should be tested before you start.
If you may be having a reaction, stop the medicine right away and get medical help. Never restart it, or any abacavir-containing medicine, after a reaction. Symptoms can return more severely within hours.
This medicine also carries a risk for people with hepatitis B. You should be tested before starting. Lamivudine-resistant hepatitis B has been reported, and severe flare-ups of hepatitis B can occur if you stop this medicine. Your liver should be closely monitored if that happens.
Patient information guide A plain-language walkthrough of Abacavir, Dolutegravir, and Lamivudine, written from its FDA label.
What Abacavir, Dolutegravir, and Lamivudine is used for
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This three-drug combination treats HIV-1 infection.
- Triumeq and Triumeq PD treat HIV-1 infection in adults.
- They are also used in pediatric patients aged at least 3 months who weigh at least 6 kg.
- They are not recommended alone if integrase inhibitor resistance is present or suspected.
How Abacavir, Dolutegravir, and Lamivudine works
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Dolutegravir is an integrase strand transfer inhibitor (INSTI). Abacavir and lamivudine are nucleoside analogue reverse transcriptase inhibitors. Together they attack HIV-1 at more than one step.
Because the dolutegravir dose in this combination is fixed, it is not enough if integrase inhibitor resistance is present.
Abacavir, Dolutegravir, and Lamivudine dosage
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Triumeq is taken by mouth once daily in adults. You can take it with or without food.
- Get tested for HLA-B*5701 and hepatitis B before starting.
- Children's dosing depends on body weight and uses Triumeq PD tablets for some weights.
- Triumeq and Triumeq PD are not interchangeable milligram for milligram.
Follow your prescriber and the label.
Dosing details from the FDA-approved label
From the Abacavir, Dolutegravir, and Lamivudine prescribing information (“Dosage and Administration”). Doses are set by your prescriber for your product, condition, kidney function and age — never change a dose on your own.
- Adults
- One tablet of TRIUMEQ daily
- May be taken with or without food
Read the label’s full dosing text
2 DOSAGE AND ADMINISTRATION • Before initiating TRIUMEQ or TRIUMEQ PD, screen for the HLA‑B*5701 allele because TRIUMEQ and TRIUMEQ PD contain abacavir. ( 2.1 ). • Prior to or when initiating TRIUMEQ or TRIUMEQ PD, test patients for HBV infection. ( 2.2 ) • TRIUMEQ and TRIUMEQ PD may be taken with or without food. ( 2.4 , 2.5 ) • Adults: One tablet of TRIUMEQ daily. ( 2.4 ) ABC = abacavir, DTG = dolutegravir, 3TC = lamivudine. Pediatric Population Body Weight Number of Tablets (once daily) Recommended Daily Dose TRIUMEQ PD Tablets (6 kg to <25 kg) 6 kg to <10 kg 3 180 mg ABC, 15 mg DTG, and 90 mg 3TC 10 kg to <14 kg 4 240 mg ABC, 20 mg DTG, and 120 mg 3TC 14 kg to <20 kg 5 300 mg ABC, 25 mg DTG, and 150 mg 3TC 20 kg to <25 kg 6 360 mg ABC, 30 mg DTG, and 180 mg 3TC TRIUMEQ Tablets (≥25 kg) ≥25 kg 1 600 mg ABC, 50 mg DTG, and 300 mg 3TC • Do not substitute TRIUMEQ and TRIUMEQ PD on a milligram-per-milligram basis. ( 2.3 ) • If dosing with certain UGT1A or CYP3A inducers, then the recommended dolutegravir dosage regimen should be adjusted. See Table 2 for complete dosing recommendations. ( 2.6 ) • Because TRIUMEQ and TRIUMEQ PD are fixed-dose tablets and cannot be dose adjusted, TRIUMEQ and TRIUMEQ PD are not recommended in patients with creatinine clearance <30 mL/min and pediatric patients with a similar degree of renal impairment based on age-appropriate assessment of renal function, or patients with hepatic impairment. ( 2.7 , 4 ) 2.1 Screening for HLA−B*5701 Allele prior to Initiating TRIUMEQ Screen for the HLA‑B*5701 allele prior to initiating therapy with TRIUMEQ or TRIUMEQ PD [see Boxed Warning , Warnings and Precautions ( 5.1 )]. 2.2 Testing prior to or When Initiating Treatment with TRIUMEQ Prior to or when initiating TRIUMEQ or TRIUMEQ PD, test patients for HBV infection [see Warnings and Precautions ( 5.2 )] . 2.3 Overview of TRIUMEQ Dosage Forms TRIUMEQ is available in two dosage forms. Do not substitute TRIUMEQ tablets and TRIUMEQ PD tablets for oral suspension on a milligram-per-milligram basis due to differing pharmacokinetic profiles for the dolutegravir component [see Warnings and Precautions ( 5.7 ) , Clinical Pharmacology ( 12.3 )] . • TRIUMEQ tablets: 600 mg of abacavir, 50 mg of dolutegravir, and 300 mg of lamivudine.
Excerpted — the section continues on the label. Read the full Dosage and Administration section on DailyMed →
Abacavir, Dolutegravir, and Lamivudine side effects
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The most commonly reported side effects in people taking Triumeq were:
Common side effects
- Trouble sleeping (insomnia)
- Headache
- Tiredness (fatigue)
When to get medical help
- Stop the medicine and get medical help right away if you suspect an allergic reaction to abacavir. Signs include fever, rash, nausea, vomiting, diarrhea, stomach pain, feeling very unwell or achy, cough, shortness of breath, or sore throat.
- Never restart this medicine, or any medicine containing abacavir, after a suspected hypersensitivity reaction. Symptoms can be worse and can lead to death within hours.
- Tell your doctor about yellow skin or eyes, dark urine, or severe stomach pain. These can signal liver problems (hepatotoxicity).
- Tell your doctor if hepatitis B symptoms flare after stopping this medicine, if you have hepatitis B.
- Report symptoms of lactic acidosis (a buildup of acid in the blood) or a severely enlarged, fatty liver. These have been seen with nucleoside analogues and can be fatal.
- Tell your doctor about new symptoms after starting HIV treatment. This may be immune reconstitution syndrome.
- Heart attack (myocardial infarction) is listed among the reported adverse reactions, so seek emergency care for heart attack symptoms.
Abacavir, Dolutegravir, and Lamivudine warnings and precautions
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- Abacavir hypersensitivity: can be fatal. Stop the medicine at once if you suspect it. Never restart afterward.
- Hepatitis B: test before starting. Severe flares can occur after stopping.
- Liver problems: liver toxicity has been reported with dolutegravir regimens, so monitoring is recommended.
- Lactic acidosis and enlarged fatty liver: reported with nucleoside analogues, including fatal cases.
- Immune reconstitution syndrome: reported with combination HIV treatment.
- Heart attack: listed among reported adverse reactions.
Abacavir, Dolutegravir, and Lamivudine interactions
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Tell your pharmacist about all your medicines. Key ones:
- Dofetilide: contraindicated because levels may rise to dangerous amounts.
- Metformin and dalfampridine: dolutegravir may raise their levels.
- Etravirine: lowers dolutegravir and is not recommended without certain boosting partners.
- Efavirenz: lowers dolutegravir, so extra dolutegravir may be needed.
- Drugs that affect UGT1A1, CYP3A, or P-gp can change dolutegravir levels.
Interactions listed in the FDA-approved label
From the Abacavir, Dolutegravir, and Lamivudine prescribing information (“Drug Interactions”): what the manufacturer studied or reported to the FDA.
- Etravirine: Decreases dolutegravir concentrations. Use of TRIUMEQ or TRIUMEQ PD with etravirine without coadministration of atazanavir/ritonavir, darunavir/ritonavir, or lopinavir/ritonavir is not recommended.
- Efavirenz: Decreases dolutegravir concentrations. In adults and in pediatric patients weighing at least 25 kg, adjust dolutegravir dose to 50 mg twice daily. An additional 50-mg dose of TIVICAY should be taken, separated by 12 hours from TRIUMEQ.
- Dofetilide, dalfampridine, and metformin (drugs eliminated via OCT2 or MATE1): Dolutegravir may increase plasma concentrations of drugs eliminated via OCT2 or MATE1. See Contraindications (4) and Drug Interactions (7.3).
- Tenofovir, methadone, midazolam, rilpivirine, and oral contraceptives containing norgestimate and ethinyl estradiol: Dolutegravir did not have a clinically relevant effect on their pharmacokinetics.
- Atazanavir, darunavir, efavirenz, etravirine, fosamprenavir, lopinavir, ritonavir, and boceprevir: Based on cross-study comparisons, dolutegravir did not appear to affect their pharmacokinetics.
- Darunavir/ritonavir, lopinavir/ritonavir, rilpivirine, tenofovir, boceprevir, prednisone, rifabutin, and omeprazole: Had no clinically significant effect on the pharmacokinetics of dolutegravir.
- Drugs that induce UGT1A1, UGT1A3, UGT1A9, CYP3A, BCRP, or P-gp: May decrease dolutegravir plasma concentrations and reduce its therapeutic effect.
- Drugs that inhibit UGT1A1, CYP3A, and related enzymes/transporters: May increase dolutegravir plasma concentrations.
Read the label’s full interactions text
7 DRUG INTERACTIONS Coadministration of TRIUMEQ or TRIUMEQ PD with other drugs can alter the concentration of other drugs and other drugs may alter the concentrations of TRIUMEQ or TRIUMEQ PD. The potential drug-drug interactions must be considered prior to and during therapy. ( 4 , 7 , 12.3 ) 7.1 Effect of Dolutegravir on the Pharmacokinetics of Other Agents In vitro, dolutegravir inhibited the renal organic cation transporters (OCT)2 (IC 50 = 1.93 microM) and multidrug and toxin extrusion transporter (MATE)1 (IC 50 = 6.34 microM). In vivo, dolutegravir inhibits tubular secretion of creatinine by inhibiting OCT2 and potentially MATE1. Dolutegravir may increase plasma concentrations of drugs eliminated via OCT2 or MATE1 (dofetilide, dalfampridine, and metformin) [see Contraindications ( 4 ), Drug Interactions ( 7.3 )] . In vitro, dolutegravir inhibited the basolateral renal transporters, organic anion transporter (OAT) 1 (IC 50 = 2.12 microM) and OAT3 (IC 50 = 1.97 microM). However, in vivo, dolutegravir did not alter the plasma concentrations of tenofovir or para-amino hippurate, substrates of OAT1 and OAT3. In vitro, dolutegravir did not inhibit (IC 50 >50 microM) the following: cytochrome P450 (CYP)1A2, CYP2A6, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP3A, uridine diphosphate (UDP)-glucuronosyl transferase (UGT)1A1, UGT2B7, P-glycoprotein (P-gp), breast cancer resistance protein (BCRP), bile salt export pump (BSEP), organic anion transporter polypeptide (OATP)1B1, OATP1B3, OCT1, or multidrug resistance protein (MRP)2, or MRP4. In vitro, dolutegravir did not induce CYP1A2, CYP2B6, CYP3A4. Based on these data and the results of drug interaction trials, dolutegravir is not expected to affect the pharmacokinetics of drugs that are substrates of these enzymes or transporters.
Excerpted — the section continues on the label. Read the full Drug Interactions section on DailyMed →
Not a complete list. The label covers the interactions the manufacturer studied or reported, and our own interaction database does not cover every medicine either. Bring your full medication list, including vitamins and herbal products, to your pharmacist.
Before taking Abacavir, Dolutegravir, and Lamivudine
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- Do not use if you carry HLA-B*5701 or have had a prior reaction to abacavir, dolutegravir, or lamivudine.
- Do not use with moderate or severe liver impairment.
- Do not use with dofetilide.
- Get tested for hepatitis B first.
- Tell your doctor about any past use of abacavir-containing medicines.
- Only for children aged at least 3 months and weighing at least 6 kg.
Abacavir, Dolutegravir, and Lamivudine overdose
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There is no known specific treatment for overdose. You would be monitored and given standard supportive care. Dialysis is unlikely to remove much dolutegravir, and it is not known whether it helps with abacavir or lamivudine.
What Abacavir, Dolutegravir, and Lamivudine does in the body
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A dedicated heart-rhythm (QT) study of dolutegravir found it did not prolong the QTc interval. Effects of abacavir, lamivudine, or the combination on QT have not been evaluated. Dolutegravir slightly lowered measured creatinine clearance in healthy volunteers, but did not significantly change actual kidney filtration.
How your body processes Abacavir, Dolutegravir, and Lamivudine
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One Triumeq tablet was bioequivalent to dolutegravir plus an abacavir/lamivudine tablet taken separately. Abacavir is absorbed quickly and has a half-life of about 1.5 hours. Dolutegravir peaks 2 to 3 hours after a dose, reaches steady state in about 5 days, and is mostly cleared through the liver and feces, with some in urine. Triumeq PD gives about 1.7-fold higher dolutegravir than Triumeq, so they are not interchangeable.
How to store Abacavir, Dolutegravir, and Lamivudine
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Store and dispense in the original package, protect from moisture, and keep the bottle tightly closed. Store at 20°C to 25°C (68°F to 77°F); excursions permitted between 15°C and 30°C (59°F to 86°F).
Written from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
Supplements & herbs that interact with Abacavir, Dolutegravir, and Lamivudine
56 supplements and herbal products have documented interactions with Abacavir, Dolutegravir, and Lamivudine in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Major · 4
- Moderate · 43
- Minor · 9
Educational information from a licensed clinical database (Natural Medicines) — see our data sources & update cadence. Not medical advice: an interaction being documented does not mean it will happen to you; do not start or stop medications or supplements without professional guidance.
Abacavir, Dolutegravir, and Lamivudine: pharmacist answers to common questions
Quick, plain-English answers to the questions patients ask most about Abacavir, Dolutegravir, and Lamivudine — the kind of thing our pharmacy team would talk through with you at the counter.
What is this medicine for?
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Why did I need blood tests before starting?
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How do I take it?
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What side effects are common?
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What symptoms mean I should stop and call right away?
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Can I stop it suddenly if I have hepatitis B too?
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Is Abacavir, Dolutegravir, and Lamivudine available over the counter?
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When was Abacavir, Dolutegravir, and Lamivudine first available?
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Answers drafted from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
More about Abacavir, Dolutegravir, and Lamivudine on HelloPharmacist
Abacavir, Dolutegravir, and Lamivudine forms and strengths (how it comes)
Abacavir, Dolutegravir, and Lamivudine is available in 1 form. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.
Tablet
How this form is used
- Triumeq treats HIV-1 infection in adults and in children aged at least 3 months and weighing at least 6 kg.
- Triumeq may be taken with or without food.
- Triumeq is taken as one tablet once daily in adults.
- Triumeq tablets and Triumeq PD tablets for oral suspension are not substitutable milligram for milligram.
Abacavir, Dolutegravir, and Lamivudine on the U.S. market: products, makers and brands
How Abacavir, Dolutegravir, and Lamivudine appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
1 company lists 2 Abacavir, Dolutegravir, and Lamivudine product records with the FDA, mostly as tablet; the earliest marketing or approval year on record is 2014. Brand names on the directory include Triumeq, Triumeq PD; the rest are generics.
Also listed with the FDA, not a patient dose form: Kit (3) — bulk drug substance sold to compounders/manufacturers and multi-item kits. These aren’t counted in the dose-form total above.
How widely Abacavir, Dolutegravir, and Lamivudine is used (Medicaid data)
A general measure of how commonly Abacavir, Dolutegravir, and Lamivudine is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q1–Q4 2025, summed across every form and brand of the drug.
Think of this as a proxy for how widely Abacavir, Dolutegravir, and Lamivudine is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.
How commonly is Abacavir, Dolutegravir, and Lamivudine prescribed? Of the 1,601 medications we measure, Abacavir, Dolutegravir, and Lamivudine ranks #630 by Medicaid prescriptions — more than 61% of them.
Utilization by Abacavir, Dolutegravir, and Lamivudine product
Pick a product to see its own Medicaid numbers. Each chip is one clinical product — a specific strength & dosage form as defined by RxNorm — with brand-name and generic versions combined.
abacavir 600 MG / dolutegravir 50 MG / lamivudine 300 MG Oral Tablet Most dispensed
Summed across the 1 of 1 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1546888
abacavir 60 MG / dolutegravir 5 MG / lamivudine 30 MG Tablet for Oral Suspension
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2598348
Shares are of the Medicaid prescriptions shown here. Product grouping follows RxNorm (the National Library of Medicine’s drug terminology), so “one product” means one strength & dosage form regardless of manufacturer. Dollar figures are gross Medicaid reimbursement before mandatory rebates — rebates (often large, especially for brand-name drugs) are confidential, so actual net cost to Medicaid is lower than shown.
Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Abacavir, Dolutegravir, and Lamivudine, and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 2 of 3 listed Abacavir, Dolutegravir, and Lamivudine NDCs with Medicaid activity.
Compare Abacavir, Dolutegravir, and Lamivudine products
A representative set of FDA-listed product records for Abacavir, Dolutegravir, and Lamivudine — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)
| Strength | Route | Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|---|---|
| 💊Tablet | ||||
| ABACAVIR SULFATE 600 mg/1; DOLUTEGRAVIR SODIUM 50 mg/1; LAMIVUDINE 300 mg | Oral | ViiV Healthcare Company | NDA | View NDC → |
| 💊Kits | ||||
| — | — | ViiV Healthcare Company | NDA | View NDC → |
Showing 2 of 2 products — FDA National Drug Code Directory. See every product, package size and price: browse all 2 Abacavir, Dolutegravir, and Lamivudine NDCs →
Abacavir, Dolutegravir, and Lamivudine side effects reported to the FDA (FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Abacavir, Dolutegravir, and Lamivudine — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Abacavir, Dolutegravir, and Lamivudine in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
Abacavir, Dolutegravir, and Lamivudine FDA approval history
How Abacavir, Dolutegravir, and Lamivudine went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
Abacavir, Dolutegravir, and Lamivudine recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
The FDA’s enforcement reports list no Abacavir, Dolutegravir, and Lamivudine recalls since July 2021.
✅No Abacavir, Dolutegravir, and Lamivudine recalls on record since July 2021Source: FDA enforcement (recall) reports, via openFDA; our copy was last updated Sep 24, 2026.
RxNorm Concept Web — From Ingredient to Every Form and Strength
This page starts with one exact multiple-ingredient concept (MIN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). A product with a different ingredient combination belongs on a different page.
RxCUI 1546887 2 dose forms · 2 strengths
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Dose form (SCDF) Oral Tablet RxCUI 1546886In current FDA listingsClinical drug / strength (SCD) abacavir 600 MG / dolutegravir 50 MG / lamivudine 300 MGRxCUI 1546888 -
Dose form (SCDF) Tablet for Oral Suspension RxCUI 2598347In current FDA listingsClinical drug / strength (SCD) abacavir 60 MG / dolutegravir 5 MG / lamivudine 30 MGRxCUI 2598348
Look up RxCUI 1546887 in the RxCUI Atlas →
RxNorm is the U.S. National Library of Medicine’s normalized drug vocabulary. Its concept hierarchy can include forms that are not currently marketed; the status on each branch compares that concept with current FDA listings. RxCUIs identify vocabulary concepts, not individual packages or manufacturers.
Abacavir, Dolutegravir, and Lamivudine supply and shortage status
Whether Abacavir, Dolutegravir, and Lamivudine is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
💵 What Abacavir, Dolutegravir, and Lamivudine costs pharmacies (NADAC benchmark)
The national average invoice price pharmacies pay for the drug itself, from CMS's NADAC survey (data as of Sep 30, 2026). This is a supply-cost benchmark — not a retail price and not what you'd pay at the counter.
| Form | Strength | Pharmacy acquisition benchmark | |
|---|---|---|---|
| Tablet, Film Coated · Oral | 600; 50; 300 mg/1; mg/1; mg | $130.01 per tablet | NDC details & price history |
| Tablet, Film Coated · Oral | ABACAVIR SULFATE 600 mg/1; DOLUTEGRAVIR SODIUM 50 mg/1; LAMIVUDINE 300 mg | $130.01 per tablet | NDC details & price history |
Source: CMS National Average Drug Acquisition Cost (NADAC), a survey of retail pharmacy invoice prices. Benchmarks shown are the range across package sizes of a representative product for each form and strength — other manufacturers' products may differ.
Abacavir, Dolutegravir, and Lamivudine brand names
Abacavir, Dolutegravir, and Lamivudine is sold under 2 brand names in the FDA directory — Triumeq, Triumeq PD. A brand and its generic contain the same active ingredient; the brand name belongs to one company's product.
Who makes Abacavir, Dolutegravir, and Lamivudine: manufacturers and labelers
One company lists Abacavir, Dolutegravir, and Lamivudine products with the FDA. By number of product records, the largest are ViiV Healthcare Company. Labelers include manufacturers and repackagers; the product in your bottle depends on which one your pharmacy stocks.
Abacavir, Dolutegravir, and Lamivudine drug class (RxNorm)
Abacavir, Dolutegravir, and Lamivudine belongs to the Human Immunodeficiency Virus Integrase Strand Transfer Inhibitor class.
Classified by RxNorm RxClass — the U.S. National Library of Medicine's standardized drug-classification service (Established Pharmacologic Class from the FDA, the ATC drug family from the WHO, and mechanism of action). Reference only, not medical advice.
Sources for this Abacavir, Dolutegravir, and Lamivudine page
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How this page is built
HelloPharmacist combines public FDA and NLM records and does not author the underlying clinical facts. The plain-language sections are written with AI from the FDA-approved label text and reviewed by our pharmacy team before publication. ViiV Healthcare Company is the representative DailyMed label linked for verification and dates. This is general education, not medical advice: always talk to your doctor or pharmacist about your own medicines. How we build and review drug pages →