Dolutegravir 50 MG / lamivudine 300 MG Oral Tablet — RxCUI 2122519
RxNorm drug concept · Semantic clinical drug
RxCUI 2122519
Semantic clinical drug · SCD
● Current RxNorm concept 1 FDA product
3 package NDCs
Snapshot Jul 14, 2026
What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.
🗂️ Key Facts
RxCUI2122519
Official nameDolutegravir 50 MG / lamivudine 300 MG Oral Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asdolutegravir 50 MG / 3TC 300 MG Oral Tablet; dolutegravir 50 MG (equivalent to 52.6 MG dolutegravir sodium) / lamivudine 300 MG Oral Tablet
FDA products mapped1
Package NDCs mapped3
Reported Medicaid activity (SDUD)103,012 prescriptions · 50 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
Our pharmacist-built guide to Dolutegravir: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
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- Can I take it with food, or does it have to be on an empty stomach?
🕸️ Concept Web — How Dolutegravir 50 MG / lamivudine 300 MG Oral Tabl... Connects
One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.
This page's concept
Dolutegravir 50 MG / lamivudine 300 MG Oral Tablet
RxCUI 2122519 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 3
The active substance itself — no strength, form, or brand attached yet.
-
Dolutegravir
1433868IN -
Lamivudine
68244IN -
Dolutegravir / lamivudine
2122518MIN
-
Dolutegravir
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Dovato
2122521BN
-
Dovato
-
Dose forms 9
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
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Dolutegravir / lamivudine Oral Tablet
2122517SCDF -
Dolutegravir / lamivudine Oral Product
2122515SCDG -
Dolutegravir / lamivudine Pill
2122516SCDG -
Dolutegravir / lamivudine Oral Tablet [Dovato]
2122523SBDF -
Dovato Oral Product
2122524SBDG -
Dovato Pill
2122525SBDG -
Oral Tablet
317541DF -
Oral Product
1151131DFG - +1 more in this family
-
Dolutegravir / lamivudine Oral Tablet
-
Clinical & branded drugs 4
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
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Dolutegravir 50 MG
1433869SCDC -
Lamivudine 300 MG
350655SCDC -
Dolutegravir 50 MG / lamivudine 300 MG Oral Tablet [Dovato]
2122526SBD -
Dolutegravir 50 MG / lamivudine 300 MG [Dovato]
2122522SBDC
-
Dolutegravir 50 MG
Showing up to 8 concepts per family — 16 of 17 stored related concepts drawn.
These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.
🔀 Generic ⇄ Brand Crosswalk
The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.
Generic (Clinical) Concepts
-
Dolutegravir 50 MG
SCDC · 1433869 -
Lamivudine 300 MG
SCDC · 350655 -
Dolutegravir / lamivudine Oral Tablet
SCDF · 2122517 -
Dolutegravir / lamivudine Oral Product
SCDG · 2122515 -
Dolutegravir / lamivudine Pill
SCDG · 2122516
Brand-Name Concepts
-
Dolutegravir 50 MG / lamivudine 300 MG Oral Tablet [Dovato]
SBD · 2122526 -
Dolutegravir 50 MG / lamivudine 300 MG [Dovato]
SBDC · 2122522 -
Dolutegravir / lamivudine Oral Tablet [Dovato]
SBDF · 2122523 -
Dovato Oral Product
SBDG · 2122524 -
Dovato Pill
SBDG · 2122525 -
Dovato
BN · 2122521
📦 FDA Products & Package NDCs
1 product · 3 package NDCs
3 package NDCs map to RxCUI 2122519 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.
| Package NDC | Package | Brand / generic name | Labeler | Marketing start |
|---|---|---|---|---|
| 49702-0246-13 | 30 TABLET, FILM COATED in 1 BOTTLE (49702-246-13) | Dovato | ViiV Healthcare Company | 2019-04-08 |
| 49702-0246-33 | 1 BLISTER PACK in 1 CARTON (49702-246-33) / 30 TABLET, FILM... | Dovato | ViiV Healthcare Company | 2024-01-01 |
| 49702-0246-62 | 1 BLISTER PACK in 1 CARTON (49702-246-62) / 14 TABLET, FILM... | Dovato | ViiV Healthcare Company | 2024-01-01 |
Observed labelers:
ViiV Healthcare Company (3)
— this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.
💲 Pricing (NADAC)
NADAC is CMS's National Average Drug Acquisition Cost — roughly what pharmacies pay to buy the drug. It is an acquisition benchmark, not your copay.
Per ea · median
$105.2550
Range $105.2550–$105.2550
· middle 50% $105.2550–$105.2550
· 2 NDCs
Latest compatible distributions from the CMS NADAC file · dataset watermark 2026-07-10. Prices vary by package and pharmacy; a distribution is shown instead of one misleading number. Rows the dataset is silent on carry no price. No zero-cost conclusion should be drawn.
🗃️ Sources & Limits
Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7
openFDA export observedJul 14, 2026
RxNorm release07/06/2026
Methodology2026-07-full-catalog-v1
- A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
- Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
- Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
- Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.