Abuse-Deterrent 12 HR oxycodone hydrochloride 80 MG Extended Release Oral Tablet — RxCUI 1860148
RxNorm drug concept · Semantic clinical drug
RxCUI 1860148
Semantic clinical drug · SCD
● Current RxNorm concept 8 FDA products
15 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
RxCUI1860148
Official nameAbuse-Deterrent 12 HR oxycodone hydrochloride 80 MG Extended Release Oral Tablet
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asoxycodone HCl 80 MG 12 HR Extended Release Oral Tablet, Abuse-Deterrent; oxyCODONE HCl 80 MG 12HR Extended Release Oral Tablet, Abuse-Deterrent
FDA products mapped8
Package NDCs mapped15
Reported Medicaid activity (SDUD)115,489 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 Oxycodone: what it is, how it’s used, side effects, and interactions.
📗 Our plain-language guide HelloPharmacist
- Extended-release oxycodone is designed for pain that's severe enough to need steady, around-the-clock control — not just occasional flare-ups. The tablet releases slowly over 12 ho...
- Why has my doctor prescribed an extended-release opioid instead of regular pain pills?
- No — and this is really important. Crushing, breaking, chewing, or dissolving the tablet destroys the controlled-release mechanism. The entire dose, meant to be released slowly ove...
- Is it okay to crush or break the tablet to make it easier to swallow?
🕸️ Concept Web — How Abuse-Deterrent 12 HR oxycodone hydrochloride 80... 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
Abuse-Deterrent 12 HR oxycodone hydrochloride 80 MG Extended Release Oral Tablet
RxCUI 1860148 Semantic clinical drug · SCD
Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.
-
Ingredients 2
The active substance itself — no strength, form, or brand attached yet.
-
Oxycodone
7804IN -
Oxycodone hydrochloride
82063PIN
-
Oxycodone
-
Brand names 1
The same medicine's trade names. A brand name alone says nothing about strength or form.
-
Oxycontin
218986BN
-
Oxycontin
-
Dose forms 13
The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.
-
Oxycodone Extended Release Oral Tablet
385094SCDF -
Oxycodone hydrochloride Extended Release Oral Tablet
2649062SCDFP -
Oxycodone Oral Product
1161682SCDG -
Oxycodone Pill
1161683SCDG -
Oxycodone hydrochloride Oral Product
2663026SCDGP -
Oxycodone hydrochloride Pill
2661812SCDGP -
Oxycodone Extended Release Oral Tablet [Oxycontin]
370158SBDF -
Oxycodone hydrochloride Extended Release Oral Tablet [Oxycontin]
2655468SBDFP - +5 more in this family
-
Oxycodone Extended Release Oral Tablet
-
Clinical & branded drugs 3
Ingredient + strength + dose form. These are the concepts real FDA products actually carry.
-
Oxycodone hydrochloride 80 MG
1049598SCDC -
Abuse-Deterrent 12 HR oxycodone hydrochloride 80 MG Extended Release Oral Tablet [Oxycontin]
1049601SBD -
Oxycodone hydrochloride 80 MG [Oxycontin]
1049600SBDC
-
Oxycodone hydrochloride 80 MG
Showing up to 8 concepts per family — 14 of 19 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
-
Oxycodone hydrochloride 80 MG
SCDC · 1049598 -
Oxycodone Extended Release Oral Tablet
SCDF · 385094 -
Oxycodone hydrochloride Extended Release Oral Tablet
SCDFP · 2649062 -
Oxycodone Oral Product
SCDG · 1161682 -
Oxycodone Pill
SCDG · 1161683 -
Oxycodone hydrochloride Oral Product
SCDGP · 2663026 -
Oxycodone hydrochloride Pill
SCDGP · 2661812
Brand-Name Concepts
-
Abuse-Deterrent 12 HR oxycodone hydrochloride 80 MG Extended Release Oral Tablet [Oxycontin]
SBD · 1049601 -
Oxycodone hydrochloride 80 MG [Oxycontin]
SBDC · 1049600 -
Oxycodone Extended Release Oral Tablet [Oxycontin]
SBDF · 370158 -
Oxycodone hydrochloride Extended Release Oral Tablet [Oxycontin]
SBDFP · 2655468 -
Oxycontin Oral Product
SBDG · 1177023 -
Oxycontin Pill
SBDG · 1177024 -
Oxycontin
BN · 218986
📦 FDA Products & Package NDCs
8 products · 15 package NDCs
15 package NDCs map to RxCUI 1860148 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 |
|---|---|---|---|---|
| 00115-1560-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLAST... | OXYCODONE HYDROCHLORIDE | Amneal Pharmaceuticals of New York LLC | 2016-02-22 |
| 59011-0410-10 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011... | OxyContin | Knoa Pharma LLC | 2010-08-08 |
| 59011-0410-20 | 2 BLISTER PACK in 1 CARTON (59011-410-20) / 10 TABLET, FILM... | OxyContin | Knoa Pharma LLC | 2010-08-08 |
| 59011-0415-10 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011... | OxyContin | Knoa Pharma LLC | 2010-08-08 |
| 59011-0415-20 | 2 BLISTER PACK in 1 CARTON (59011-415-20) / 10 TABLET, FILM... | OxyContin | Knoa Pharma LLC | 2010-08-08 |
| 59011-0420-10 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011... | OxyContin | Knoa Pharma LLC | 2010-08-08 |
| 59011-0420-20 | 2 BLISTER PACK in 1 CARTON (59011-420-20) / 10 TABLET, FILM... | OxyContin | Knoa Pharma LLC | 2010-08-08 |
| 59011-0430-10 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011... | OxyContin | Knoa Pharma LLC | 2010-08-08 |
| 59011-0430-20 | 2 BLISTER PACK in 1 CARTON (59011-430-20) / 10 TABLET, FILM... | OxyContin | Knoa Pharma LLC | 2010-08-08 |
| 59011-0440-10 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011... | OxyContin | Knoa Pharma LLC | 2010-08-08 |
| 59011-0440-20 | 2 BLISTER PACK in 1 CARTON (59011-440-20) / 10 TABLET, FILM... | OxyContin | Knoa Pharma LLC | 2010-08-08 |
| 59011-0460-10 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011... | OxyContin | Knoa Pharma LLC | 2010-08-08 |
| 59011-0460-20 | 2 BLISTER PACK in 1 CARTON (59011-460-20) / 10 TABLET, FILM... | OxyContin | Knoa Pharma LLC | 2010-08-08 |
| 59011-0480-10 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011... | OxyContin | Knoa Pharma LLC | 2010-08-08 |
| 59011-0480-20 | 2 BLISTER PACK in 1 CARTON (59011-480-20) / 10 TABLET, FILM... | OxyContin | Knoa Pharma LLC | 2010-08-08 |
Observed labelers:
Knoa Pharma LLC (14) ·
Amneal Pharmaceuticals of New York LLC (1)
— 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.