Buprenorphine 11.4 MG / naloxone 2.9 MG Sublingual Tablet [Zubsolv] — RxCUI 1597570
RxNorm drug concept · Semantic branded drug
RxCUI 1597570
Semantic branded drug · SBD
● Current RxNorm concept 12 FDA products
12 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
RxCUI1597570
Official nameBuprenorphine 11.4 MG / naloxone 2.9 MG Sublingual Tablet [Zubsolv]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known aszubsolv 11.4 MG / 2.9 MG Sublingual Tablet
FDA products mapped12
Package NDCs mapped12
Reported Medicaid activity (SDUD)115,191 prescriptions · 44 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026
📖 Skip the Codes — Read It in Plain English.
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📗 Our plain-language guide HelloPharmacist
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🕸️ Concept Web — How Buprenorphine 11.4 MG / naloxone 2.9 MG Sublingu... 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
Buprenorphine 11.4 MG / naloxone 2.9 MG Sublingual Tablet [Zubsolv]
RxCUI 1597570 Semantic branded drug · SBD
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.
-
Buprenorphine
1819IN -
Naloxone
7242IN -
Buprenorphine / naloxone
352364MIN
-
Buprenorphine
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Zubsolv
1431077BN
-
Zubsolv
-
Dose forms 12
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
-
Buprenorphine / naloxone Sublingual Tablet
378762SCDF -
Buprenorphine / naloxone Oral Product
1151359SCDG -
Buprenorphine / naloxone Pill
1151360SCDG -
Buprenorphine / naloxone Sublingual Product
1294831SCDG -
Buprenorphine / naloxone Sublingual Tablet [Zubsolv]
1431079SBDF -
Zubsolv Oral Product
1431080SBDG -
Zubsolv Pill
1431081SBDG -
Zubsolv Sublingual Product
1431082SBDG - +4 more in this family
-
Buprenorphine / naloxone Sublingual Tablet
-
Clinical & branded drugs 4
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
-
Buprenorphine 11.4 MG / naloxone 2.9 MG Sublingual Tablet
1597568SCD -
Buprenorphine 11.4 MG
1597566SCDC -
Naloxone 2.9 MG
1597567SCDC -
Buprenorphine 11.4 MG / naloxone 2.9 MG [Zubsolv]
1597569SBDC
-
Buprenorphine 11.4 MG / naloxone 2.9 MG Sublingual Tablet
Showing up to 8 concepts per family — 16 of 20 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
-
Buprenorphine 11.4 MG / naloxone 2.9 MG Sublingual Tablet
SCD · 1597568 -
Buprenorphine 11.4 MG
SCDC · 1597566 -
Naloxone 2.9 MG
SCDC · 1597567 -
Buprenorphine / naloxone Sublingual Tablet
SCDF · 378762 -
Buprenorphine / naloxone Oral Product
SCDG · 1151359 -
Buprenorphine / naloxone Pill
SCDG · 1151360 -
Buprenorphine / naloxone Sublingual Product
SCDG · 1294831
Brand-Name Concepts
-
Buprenorphine 11.4 MG / naloxone 2.9 MG [Zubsolv]
SBDC · 1597569 -
Buprenorphine / naloxone Sublingual Tablet [Zubsolv]
SBDF · 1431079 -
Zubsolv Oral Product
SBDG · 1431080 -
Zubsolv Pill
SBDG · 1431081 -
Zubsolv Sublingual Product
SBDG · 1431082 -
Zubsolv
BN · 1431077
📦 FDA Products & Package NDCs
12 products · 12 package NDCs
12 package NDCs map to RxCUI 1597570 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 |
|---|---|---|---|---|
| 54123-0114-30 | 3 BLISTER PACK in 1 CARTON (54123-114-30) / 10 TABLET, ORAL... | Zubsolv | Orexo US, Inc. | 2014-12-11 |
| 54123-0907-30 | 3 BLISTER PACK in 1 CARTON (54123-907-30) / 10 TABLET, ORAL... | Zubsolv | Orexo US, Inc. | 2013-07-04 |
| 54123-0914-30 | 3 BLISTER PACK in 1 CARTON (54123-914-30) / 10 TABLET, ORAL... | Zubsolv | Orexo US, Inc. | 2013-07-04 |
| 54123-0929-30 | 3 BLISTER PACK in 1 CARTON (54123-929-30) / 10 TABLET, ORAL... | Zubsolv | Orexo US, Inc. | 2013-07-04 |
| 54123-0957-30 | 3 BLISTER PACK in 1 CARTON (54123-957-30) / 10 TABLET, ORAL... | Zubsolv | Orexo US, Inc. | 2013-07-04 |
| 54123-0986-30 | 3 BLISTER PACK in 1 CARTON (54123-986-30) / 10 TABLET, ORAL... | Zubsolv | Orexo US, Inc. | 2014-12-11 |
| 82111-0201-30 | 3 BLISTER PACK in 1 CARTON (82111-201-30) / 10 TABLET, ORAL... | Zubsolv | Edenbridge Pharmaceuticals LLC. | 2026-06-12 |
| 82111-0202-30 | 3 BLISTER PACK in 1 CARTON (82111-202-30) / 10 TABLET, ORAL... | Zubsolv | Edenbridge Pharmaceuticals LLC. | 2026-06-12 |
| 82111-0203-30 | 3 BLISTER PACK in 1 CARTON (82111-203-30) / 10 TABLET, ORAL... | Zubsolv | Edenbridge Pharmaceuticals LLC. | 2026-06-12 |
| 82111-0204-30 | 3 BLISTER PACK in 1 CARTON (82111-204-30) / 10 TABLET, ORAL... | Zubsolv | Edenbridge Pharmaceuticals LLC. | 2026-06-12 |
| 82111-0205-30 | 3 BLISTER PACK in 1 CARTON (82111-205-30) / 10 TABLET, ORAL... | Zubsolv | Edenbridge Pharmaceuticals LLC. | 2026-06-12 |
| 82111-0206-30 | 3 BLISTER PACK in 1 CARTON (82111-206-30) / 10 TABLET, ORAL... | Zubsolv | Edenbridge Pharmaceuticals LLC. | 2026-06-12 |
Observed labelers:
Edenbridge Pharmaceuticals LLC. (6) ·
Orexo US, Inc. (6)
— this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.
🗃️ 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.